Variant report

Variant	rs4980526
Chromosome Location	chr11:63952396-63952397
allele	C/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	HEY1	chr11:63951779-63953349	K562	blood:	n/a	chr11:63953122-63953137 chr11:63952939-63952954
2	POLR2A	chr11:63951929-63953907	Raji	blood:	n/a	n/a
3	HMGN3	chr11:63952362-63953263	K562	blood:	n/a	n/a
4	HEY1	chr11:63952201-63952565	HepG2	liver:	n/a	n/a
5	POLR2A	chr11:63950154-63954471	SK-N-MC	brain:	n/a	n/a
6	TBP	chr11:63952032-63953829	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr11:63952302-63953783	Hela-S3	cervix:	n/a	n/a
8	TCF7L2	chr11:63952090-63953676	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr11:63952382-63953301	ECC-1	luminal epithelium:	n/a	n/a
10	HEY1	chr11:63952185-63952570	HepG2	liver:	n/a	n/a
11	POLR2A	chr11:63952369-63953326	GM12878	blood:	n/a	n/a
12	TCF7L2	chr11:63952277-63953835	HCT-116	colon:	n/a	n/a
13	POLR2A	chr11:63952297-63953870	K562	blood:	n/a	n/a
14	POLR2A	chr11:63952192-63953825	Hela-S3	cervix:	n/a	n/a
15	MAX	chr11:63952137-63953879	NB4	blood:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
16	RCOR1	chr11:63952235-63953106	K562	blood:	n/a	n/a
17	MYC	chr11:63952186-63953877	K562	blood:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
18	MAX	chr11:63952273-63953888	K562	blood:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
19	POLR2A	chr11:63952185-63952550	ECC-1	luminal epithelium:	n/a	n/a
20	CTCF	chr11:63952300-63952450	Caco-2	colon:	n/a	n/a
21	RCOR1	chr11:63952150-63953797	K562	blood:	n/a	n/a
22	MAX	chr11:63952297-63953851	A549	lung:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
23	POLR2A	chr11:63950640-63953983	PFSK-1	brain:	n/a	n/a
24	MAX	chr11:63952315-63953850	SK-N-SH	brain:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
25	CHD1	chr11:63952126-63953117	H1-hESC	embryonic stem cell:	n/a	n/a
26	BHLHE40	chr11:63952392-63953853	HepG2	liver:	n/a	chr11:63953125-63953141
27	MXI1	chr11:63952006-63955085	IMR90	lung:	n/a	chr11:63952886-63952895 chr11:63952326-63952335
28	USF2	chr11:63952371-63953202	H1-hESC	embryonic stem cell:	n/a	chr11:63952885-63952896 chr11:63953125-63953141
29	POLR2A	chr11:63952019-63953980	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr11:63951744-63954981	K562	blood:	n/a	n/a
31	REST	chr11:63952069-63954104	H1-neurons	neurons:	n/a	chr11:63952981-63952994
32	MAX	chr11:63951922-63954341	K562	blood:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
33	POLR2A	chr11:63952349-63953888	GM19099	blood:	n/a	n/a
34	MAX	chr11:63952305-63953886	MCF-7	breast:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
35	POLR2A	chr11:63952379-63953300	A549	lung:	n/a	n/a
36	MAX	chr11:63952361-63953851	GM12878	blood:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
37	CCNT2	chr11:63952305-63954672	K562	blood:	n/a	chr11:63954092-63954101 chr11:63953748-63953757 chr11:63954444-63954453 chr11:63953183-63953192 chr11:63954115-63954124 chr11:63953037-63953046
38	MAX	chr11:63952257-63953946	H1-hESC	embryonic stem cell:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
39	JUND	chr11:63952261-63952530	K562	blood:	n/a	n/a
40	E2F6	chr11:63952035-63953994	A549	lung:	n/a	chr11:63953127-63953137
41	POLR2A	chr11:63952216-63953277	K562	blood:	n/a	n/a
42	MAX	chr11:63952134-63953984	A549	lung:	n/a	chr11:63952885-63952898 chr11:63952887-63952896 chr11:63952887-63952896
43	ZNF384	chr11:63952010-63952457	GM12878	blood:	n/a	n/a
44	POLR2A	chr11:63952328-63953947	HUVEC	blood vessel:	n/a	n/a
45	CREB1	chr11:63952192-63953977	HepG2	liver:	n/a	chr11:63952885-63952898
46	USF2	chr11:63952224-63953570	Hela-S3	cervix:	n/a	chr11:63952885-63952896 chr11:63953125-63953141
47	TCF7L2	chr11:63952263-63952543	MCF-7	breast:	n/a	n/a
48	ARID3A	chr11:63952392-63952599	K562	blood:	n/a	n/a
49	POLR2A	chr11:63952098-63953947	PANC-1	pancreas:	n/a	n/a
50	EP300	chr11:63951987-63953950	SK-N-SH	brain:	n/a	chr11:63953524-63953533

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	chr11:63929801..63939249-chr11:63945151..63958671,77	MCF-7	breast:
4	chr11:63950964..63952504-chr11:64109003..64111776,2	K562	blood:
5	chr11:63951436..63953317-chr11:64064136..64066552,3	MCF-7	breast:
6	chr11:63765241..63769899-chr11:63951624..63954334,5	MCF-7	breast:
7	chr11:63951654..63956341-chr11:63991514..63996131,9	MCF-7	breast:
8	chr11:63929784..63936274-chr11:63944807..63955078,25	K562	blood:
9	chr11:63949228..63955854-chr11:64049902..64053814,7	MCF-7	breast:
10	chr11:63929784..63936174-chr11:63947045..63954638,30	K562	blood:
11	chr11:63951739..63953633-chr11:64084180..64087217,3	MCF-7	breast:
12	chr1:32478963..32479613-chr11:63952297..63953257,2	HCT-116	colon:
13	chr11:62605946..62608654-chr11:63950843..63953926,3	MCF-7	breast:
14	chr11:63752327..63755463-chr11:63951684..63954508,4	MCF-7	breast:
15	chr11:63931311..63936745-chr11:63945647..63958123,49	MCF-7	breast:
16	chr11:63951267..63954594-chr11:64105049..64110612,5	MCF-7	breast:
17	chr11:63742089..63743658-chr11:63951371..63953619,2	K562	blood:
18	chr11:63951371..63956321-chr11:64011600..64016157,10	MCF-7	breast:
19	chr11:63951667..63955297-chr11:64041322..64044678,4	MCF-7	breast:
20	chr11:63951620..63954482-chr11:64017344..64021444,4	MCF-7	breast:
21	chr11:63951359..63955952-chr11:63973161..63976481,4	MCF-7	breast:
22	chr11:63951070..63956024-chr11:64006485..64011246,10	MCF-7	breast:
23	chr11:63952347..63953312-chr12:109124679..109125459,2	Hela-S3	cervix:
24	chr11:63952189..63953757-chr11:64081280..64082901,2	K562	blood:
25	chr11:63950774..63958537-chr11:64070493..64074690,13	MCF-7	breast:
26	chr11:63951087..63956474-chr11:63963164..63967847,7	MCF-7	breast:
27	chr11:63950870..63952881-chr11:64001401..64003560,2	MCF-7	breast:
28	chr11:63951617..63953554-chr11:64071921..64074266,2	MCF-7	breast:
29	chr11:63654599..63657425-chr11:63952225..63954812,2	K562	blood:
30	chr11:63951738..63954910-chr11:63969305..63972187,3	MCF-7	breast:
31	chr11:63753400..63755949-chr11:63951622..63955787,3	K562	blood:
32	chr11:63952254..63954139-chr11:64052656..64054498,2	MCF-7	breast:
33	chr11:63951708..63954659-chr11:63996505..63999341,3	MCF-7	breast:

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

Variant related genes	Relation type
STIP1	TF binding region
ENSG00000149781	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000256100	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000149761	Chromatin interaction
ENSG00000198518	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000173511	Chromatin interaction
ENSG00000110880	Chromatin interaction
ENSG00000173457	Chromatin interaction
ENSG00000256940	Chromatin interaction
ENSG00000110583	Chromatin interaction
ENSG00000110011	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000121774	Chromatin interaction
ENSG00000256116	Chromatin interaction
ENSG00000167770	Chromatin interaction
ENSG00000149743	Chromatin interaction
ENSG00000149782	Chromatin interaction
ENSG00000182450	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000173486	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000072518	Chromatin interaction
ENSG00000168071	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs2246552	1.00[AMR][1000 genomes]
rs2254599	0.85[AMR][1000 genomes]
rs2254709	0.85[AMR][1000 genomes]
rs2325785	1.00[AMR][1000 genomes]
rs2429457	1.00[AFR][1000 genomes]
rs2508208	0.89[AFR][1000 genomes]
rs2515239	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2515240	0.97[AFR][1000 genomes]
rs2622413	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2622414	1.00[AMR][1000 genomes]
rs2622415	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2622416	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2622421	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2622423	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2622431	0.85[AMR][1000 genomes]
rs2701525	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2701526	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2701528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2701529	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2701532	1.00[AMR][1000 genomes]
rs2701535	1.00[AMR][1000 genomes]
rs2701538	1.00[AMR][1000 genomes]
rs2845587	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2845589	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2845591	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2845595	1.00[AMR][1000 genomes]
rs2845598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35525149	1.00[AFR][1000 genomes]
rs4294564	1.00[AFR][1000 genomes]
rs4587731	1.00[AFR][1000 genomes]
rs60647009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs611637	0.93[AFR][1000 genomes]
rs620818	0.93[AFR][1000 genomes]
rs633557	0.95[AFR][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

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63949200-63952400	Enhancers	Lung	lung
2	chr11:63950800-63953000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
3	chr11:63951000-63952600	Enhancers	Spleen	Spleen
4	chr11:63951000-63953000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr11:63951200-63952400	Enhancers	Stomach Mucosa	stomach
6	chr11:63951200-63953200	Flanking Active TSS	Stomach Smooth Muscle	stomach
7	chr11:63951200-63955200	Active TSS	H9 Cell Line	embryonic stem cell
8	chr11:63951400-63952400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:63951400-63952400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:63951400-63952400	Enhancers	Fetal Brain Male	brain
11	chr11:63951400-63952800	Flanking Active TSS	Dnd41	blood
12	chr11:63951400-63952800	Flanking Active TSS	HepG2	liver
13	chr11:63951600-63952400	Weak transcription	Aorta	Aorta
14	chr11:63951600-63952400	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr11:63951600-63952400	Weak transcription	Small Intestine	intestine
16	chr11:63951600-63952600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr11:63951600-63954800	Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr11:63951600-63954800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:63951800-63952400	Enhancers	Primary B cells from peripheral blood	blood
20	chr11:63951800-63952400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr11:63951800-63952400	Enhancers	Placenta Amnion	Placenta Amnion
22	chr11:63951800-63952600	Flanking Active TSS	Brain Hippocampus Middle	brain
23	chr11:63951800-63952800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr11:63951800-63952800	Flanking Active TSS	Rectal Smooth Muscle	rectum
25	chr11:63951800-63953000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr11:63951800-63953200	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr11:63951800-63954400	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr11:63951800-63954600	Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr11:63951800-63954600	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr11:63951800-63954600	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr11:63952000-63952400	Active TSS	H1 Cell Line	embryonic stem cell
32	chr11:63952000-63952400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:63952000-63952400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr11:63952000-63952400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr11:63952000-63952400	Flanking Active TSS	Psoas Muscle	Psoas
36	chr11:63952000-63952400	Flanking Active TSS	HSMMtube	muscle
37	chr11:63952000-63952600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:63952000-63952600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr11:63952000-63952600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr11:63952000-63952600	Flanking Active TSS	Brain Substantia Nigra	brain
41	chr11:63952000-63952600	Flanking Active TSS	Fetal Stomach	stomach
42	chr11:63952000-63952600	Flanking Active TSS	NHEK	skin
43	chr11:63952000-63952800	Flanking Active TSS	Colonic Mucosa	Colon
44	chr11:63952000-63952800	Flanking Active TSS	Duodenum Mucosa	Duodenum
45	chr11:63952000-63952800	Flanking Active TSS	Fetal Brain Female	brain
46	chr11:63952000-63952800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
47	chr11:63952000-63952800	Flanking Active TSS	HUVEC	blood vessel
48	chr11:63952000-63952800	Flanking Active TSS	NH-A	brain
49	chr11:63952000-63953000	Flanking Active TSS	Primary B cells from cord blood	blood
50	chr11:63952000-63953000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood

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