Variant report

Variant	rs7941773
Chromosome Location	chr11:63952759-63952760
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:370)
CpG islands
(count:0)
Chromatin interactive
region (count:48)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:63952661-63953296	SK-N-SH	brain:	n/a	n/a
2	HEY1	chr11:63951779-63953349	K562	blood:	n/a	chr11:63953122-63953137 chr11:63952939-63952954
3	BHLHE40	chr11:63952437-63953852	K562	blood:	n/a	chr11:63953125-63953141
4	POLR2A	chr11:63951929-63953907	Raji	blood:	n/a	n/a
5	HMGN3	chr11:63952362-63953263	K562	blood:	n/a	n/a
6	POLR2A	chr11:63950154-63954471	SK-N-MC	brain:	n/a	n/a
7	MYC	chr11:63952695-63953052	MCF-7	breast:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
8	TBP	chr11:63952032-63953829	H1-hESC	embryonic stem cell:	n/a	n/a
9	PPARGC1A	chr11:63952598-63953831	HepG2	liver:	n/a	n/a
10	BRCA1	chr11:63952302-63953783	Hela-S3	cervix:	n/a	n/a
11	TCF7L2	chr11:63952090-63953676	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr11:63952382-63953301	ECC-1	luminal epithelium:	n/a	n/a
13	SIN3AK20	chr11:63952727-63953253	HepG2	liver:	n/a	n/a
14	PML	chr11:63952434-63953833	GM12878	blood:	n/a	n/a
15	POLR2A	chr11:63952369-63953326	GM12878	blood:	n/a	n/a
16	REST	chr11:63952611-63953935	A549	lung:	n/a	chr11:63952981-63952994
17	TCF7L2	chr11:63952277-63953835	HCT-116	colon:	n/a	n/a
18	ELF1	chr11:63952731-63953799	HepG2	liver:	n/a	chr11:63952944-63952956
19	POLR2A	chr11:63952297-63953870	K562	blood:	n/a	n/a
20	CTCF	chr11:63952626-63953852	IMR90	lung:	n/a	chr11:63953658-63953671 chr11:63953656-63953672
21	POLR2A	chr11:63952192-63953825	Hela-S3	cervix:	n/a	n/a
22	MAX	chr11:63952137-63953879	NB4	blood:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
23	RCOR1	chr11:63952235-63953106	K562	blood:	n/a	n/a
24	PML	chr11:63952695-63953895	K562	blood:	n/a	n/a
25	BHLHE40	chr11:63952588-63953867	GM12878	blood:	n/a	chr11:63953125-63953141
26	EP300	chr11:63952735-63953798	K562	blood:	n/a	chr11:63953524-63953533
27	PML	chr11:63952592-63953399	MCF-7	breast:	n/a	n/a
28	RAD21	chr11:63952511-63953114	IMR90	lung:	n/a	chr11:63952924-63952934
29	POLR2A	chr11:63952514-63953860	HUVEC	blood vessel:	n/a	n/a
30	USF1	chr11:63952532-63953153	ECC-1	luminal epithelium:	n/a	chr11:63952885-63952896 chr11:63953125-63953141
31	POLR2A	chr11:63952534-63953907	GM18526	blood:	n/a	n/a
32	TAF1	chr11:63952718-63953863	MCF-7	breast:	n/a	n/a
33	MYC	chr11:63952186-63953877	K562	blood:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
34	MAX	chr11:63952273-63953888	K562	blood:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
35	HEY1	chr11:63952618-63953298	HepG2	liver:	n/a	chr11:63953122-63953137 chr11:63952939-63952954
36	TCF12	chr11:63952630-63953306	A549	lung:	n/a	n/a
37	POLR2A	chr11:63952486-63953906	GM12892	blood:	n/a	n/a
38	MXI1	chr11:63952499-63953755	H1-hESC	embryonic stem cell:	n/a	chr11:63952886-63952895
39	HEY1	chr11:63952591-63953328	K562	blood:	n/a	chr11:63953122-63953137 chr11:63952939-63952954
40	TAF7	chr11:63952728-63953244	H1-hESC	embryonic stem cell:	n/a	n/a
41	RCOR1	chr11:63952150-63953797	K562	blood:	n/a	n/a
42	SP4	chr11:63952675-63953772	H1-hESC	embryonic stem cell:	n/a	chr11:63953614-63953630 chr11:63953180-63953196 chr11:63953414-63953425 chr11:63953743-63953759
43	MAX	chr11:63952297-63953851	A549	lung:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
44	CTCF	chr11:63952700-63952850	GM06990	blood:	n/a	n/a
45	POLR2A	chr11:63950640-63953983	PFSK-1	brain:	n/a	n/a
46	MAX	chr11:63952315-63953850	SK-N-SH	brain:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
47	CHD1	chr11:63952126-63953117	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr11:63952663-63953325	HCT-116	colon:	n/a	n/a
49	BHLHE40	chr11:63952392-63953853	HepG2	liver:	n/a	chr11:63953125-63953141
50	ELF1	chr11:63952661-63953139	HepG2	liver:	n/a	chr11:63952944-63952956

No data

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:63704888..63707484-chr11:63951709..63953319,2	MCF-7	breast:
2	chr11:63951584..63953989-chr6:26204778..26206338,2	MCF-7	breast:
3	chr11:63952495..63953312-chr2:68479228..68479768,2	Hela-S3	cervix:
4	chr11:63929801..63939249-chr11:63945151..63958671,77	MCF-7	breast:
5	chr11:63951436..63953317-chr11:64064136..64066552,3	MCF-7	breast:
6	chr11:63765241..63769899-chr11:63951624..63954334,5	MCF-7	breast:
7	chr11:63605595..63608737-chr11:63952425..63954944,4	MCF-7	breast:
8	chr11:63952434..63954296-chr17:57918251..57920661,2	MCF-7	breast:
9	chr11:63952667..63953169-chr13:52026699..52027319,2	NB4	blood:
10	chr11:63951654..63956341-chr11:63991514..63996131,9	MCF-7	breast:
11	chr11:63929784..63936274-chr11:63944807..63955078,25	K562	blood:
12	chr11:63949228..63955854-chr11:64049902..64053814,7	MCF-7	breast:
13	chr11:63929784..63936174-chr11:63947045..63954638,30	K562	blood:
14	chr11:63951739..63953633-chr11:64084180..64087217,3	MCF-7	breast:
15	chr1:32478963..32479613-chr11:63952297..63953257,2	HCT-116	colon:
16	chr11:63952709..63953353-chr19:39926267..39927257,2	HCT-116	colon:
17	chr11:62605946..62608654-chr11:63950843..63953926,3	MCF-7	breast:
18	chr11:63752327..63755463-chr11:63951684..63954508,4	MCF-7	breast:
19	chr11:63952535..63953481-chr6:2841684..2842219,2	Hela-S3	cervix:
20	chr11:63931311..63936745-chr11:63945647..63958123,49	MCF-7	breast:
21	chr11:63951267..63954594-chr11:64105049..64110612,5	MCF-7	breast:
22	chr11:63742089..63743658-chr11:63951371..63953619,2	K562	blood:
23	chr11:63951371..63956321-chr11:64011600..64016157,10	MCF-7	breast:
24	chr11:63952660..63953163-chr12:6976657..6977189,2	NB4	blood:
25	chr11:63952700..63953235-chr16:4475506..4476291,2	MCF-7	breast:
26	chr11:63951667..63955297-chr11:64041322..64044678,4	MCF-7	breast:
27	chr11:63951620..63954482-chr11:64017344..64021444,4	MCF-7	breast:
28	chr11:63951359..63955952-chr11:63973161..63976481,4	MCF-7	breast:
29	chr11:63951070..63956024-chr11:64006485..64011246,10	MCF-7	breast:
30	chr1:150208017..150208704-chr11:63952439..63953325,2	Hela-S3	cervix:
31	chr11:63952347..63953312-chr12:109124679..109125459,2	Hela-S3	cervix:
32	chr11:63952189..63953757-chr11:64081280..64082901,2	K562	blood:
33	chr1:45186939..45187886-chr11:63952731..63953389,2	Hela-S3	cervix:
34	chr11:63952707..63953213-chr19:12661901..12662858,2	NB4	blood:
35	chr11:63950774..63958537-chr11:64070493..64074690,13	MCF-7	breast:
36	chr11:63952707..63953255-chr17:16341877..16342799,2	HCT-116	colon:
37	chr10:112631537..112632160-chr11:63952691..63953645,2	NB4	blood:
38	chr11:63951087..63956474-chr11:63963164..63967847,7	MCF-7	breast:
39	chr11:63950870..63952881-chr11:64001401..64003560,2	MCF-7	breast:
40	chr11:63951617..63953554-chr11:64071921..64074266,2	MCF-7	breast:
41	chr11:63952607..63955696-chr11:64083637..64087133,4	K562	blood:
42	chr11:63952633..63953314-chr6:43139325..43140219,2	Hela-S3	cervix:
43	chr11:63952489..63953478-chr3:25824457..25825585,3	Hela-S3	cervix:
44	chr11:63654599..63657425-chr11:63952225..63954812,2	K562	blood:
45	chr11:63951738..63954910-chr11:63969305..63972187,3	MCF-7	breast:
46	chr11:63753400..63755949-chr11:63951622..63955787,3	K562	blood:
47	chr11:63952254..63954139-chr11:64052656..64054498,2	MCF-7	breast:
48	chr11:63951708..63954659-chr11:63996505..63999341,3	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MACROD1-2	chr11:63950298-63953164	NONHSAT021947

No data

Variant related genes	Relation type
STIP1	TF binding region
ENSG00000173264	Chromatin interaction
ENSG00000110011	Chromatin interaction
ENSG00000198518	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000149743	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000110880	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000182450	Chromatin interaction
ENSG00000256940	Chromatin interaction
ENSG00000149781	Chromatin interaction
ENSG00000072518	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000173457	Chromatin interaction
ENSG00000121774	Chromatin interaction
ENSG00000196235	Chromatin interaction
ENSG00000256116	Chromatin interaction
ENSG00000167770	Chromatin interaction
ENSG00000149782	Chromatin interaction
ENSG00000150593	Chromatin interaction
ENSG00000173511	Chromatin interaction
ENSG00000151092	Chromatin interaction
ENSG00000112658	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000151093	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000021355	Chromatin interaction
ENSG00000262246	Chromatin interaction
ENSG00000111669	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000102786	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000173486	Chromatin interaction
ENSG00000196826	Chromatin interaction
ENSG00000256100	Chromatin interaction
ENSG00000143401	Chromatin interaction
ENSG00000221823	Chromatin interaction
ENSG00000103423	Chromatin interaction
ENSG00000203497	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000249709	Chromatin interaction
ENSG00000110583	Chromatin interaction
ENSG00000175061	Chromatin interaction
ENSG00000149761	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000105193	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1011219	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11231710	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11231713	0.89[EUR][1000 genomes]
rs11231726	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11600628	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11600667	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11604083	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11605193	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11605856	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11607903	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12417635	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12419038	0.90[ASN][1000 genomes]
rs17773078	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2005272	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2096706	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2186572	0.87[EUR][1000 genomes]
rs3862371	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55942618	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55970968	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56207008	0.90[EUR][1000 genomes]
rs56311067	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57021319	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60394481	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7103915	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7109921	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7122408	0.80[EUR][1000 genomes]
rs7123026	0.88[EUR][1000 genomes]
rs734762	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs947939	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 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	nsv832185	chr11:63819946-63963532	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	89 gene(s)	inside rSNPs	diseases
6	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
7	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
8	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
9	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
10	nsv897663	chr11:63910153-63962152	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	86 gene(s)	inside rSNPs	n/a
11	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
12	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
13	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
14	nsv897665	chr11:63927695-64026144	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised 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	155 gene(s)	inside rSNPs	diseases
15	nsv897666	chr11:63929493-64026144	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
16	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
17	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
18	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
19	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7941773	NUDT22	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63950800-63953000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
2	chr11:63951000-63953000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
3	chr11:63951200-63953200	Flanking Active TSS	Stomach Smooth Muscle	stomach
4	chr11:63951200-63955200	Active TSS	H9 Cell Line	embryonic stem cell
5	chr11:63951400-63952800	Flanking Active TSS	Dnd41	blood
6	chr11:63951400-63952800	Flanking Active TSS	HepG2	liver
7	chr11:63951600-63954800	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr11:63951600-63954800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:63951800-63952800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr11:63951800-63952800	Flanking Active TSS	Rectal Smooth Muscle	rectum
11	chr11:63951800-63953000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr11:63951800-63953200	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr11:63951800-63954400	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr11:63951800-63954600	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr11:63951800-63954600	Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr11:63951800-63954600	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr11:63952000-63952800	Flanking Active TSS	Colonic Mucosa	Colon
18	chr11:63952000-63952800	Flanking Active TSS	Duodenum Mucosa	Duodenum
19	chr11:63952000-63952800	Flanking Active TSS	Fetal Brain Female	brain
20	chr11:63952000-63952800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
21	chr11:63952000-63952800	Flanking Active TSS	HUVEC	blood vessel
22	chr11:63952000-63952800	Flanking Active TSS	NH-A	brain
23	chr11:63952000-63953000	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr11:63952000-63953000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
25	chr11:63952000-63953000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:63952000-63953000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr11:63952000-63953000	Flanking Active TSS	Fetal Muscle Leg	muscle
28	chr11:63952000-63953000	Flanking Active TSS	HMEC	breast
29	chr11:63952000-63953000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr11:63952000-63953200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:63952000-63953200	Active TSS	Fetal Kidney	kidney
32	chr11:63952000-63954600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:63952000-63954600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr11:63952000-63954600	Active TSS	Right Atrium	heart
35	chr11:63952000-63954600	Active TSS	A549	lung
36	chr11:63952000-63955200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr11:63952200-63952800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr11:63952200-63952800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr11:63952200-63952800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
40	chr11:63952200-63952800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
41	chr11:63952200-63952800	Flanking Active TSS	Primary T cells from cord blood	blood
42	chr11:63952200-63952800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
43	chr11:63952200-63952800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
44	chr11:63952200-63952800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr11:63952200-63952800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
46	chr11:63952200-63952800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
47	chr11:63952200-63952800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr11:63952200-63952800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:63952200-63952800	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr11:63952200-63952800	Flanking Active TSS	Liver	Liver

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