Variant report

Variant	rs680273
Chromosome Location	chr11:64539635-64539636
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:35)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:35 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MXI1	chr11:64539376-64539697	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:64538863-64539647	K562	blood:	n/a	n/a
3	POLR2A	chr11:64525013-64542071	HepG2	liver:	n/a	n/a
4	POLR2A	chr11:64533761-64543234	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:64538757-64539758	PFSK-1	brain:	n/a	n/a
6	POLR2A	chr11:64539454-64540026	A549	lung:	n/a	n/a
7	POLR2A	chr11:64538799-64539885	SK-N-MC	brain:	n/a	n/a
8	POLR2A	chr11:64539382-64539656	GM12891	blood:	n/a	n/a
9	SPI1	chr11:64539329-64539724	GM12891	blood:	n/a	n/a
10	BCLAF1	chr11:64539256-64539869	GM12878	blood:	n/a	chr11:64539560-64539569
11	POLR2A	chr11:64538728-64540087	GM12892	blood:	n/a	n/a
12	POLR2A	chr11:64538779-64539738	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr11:64539265-64539746	GM12891	blood:	n/a	n/a
14	POLR2A	chr11:64539389-64539640	K562	blood:	n/a	n/a
15	NFATC1	chr11:64539477-64540491	GM12878	blood:	n/a	n/a
16	MEF2A	chr11:64539493-64540578	GM12878	blood:	n/a	n/a
17	POLR2A	chr11:64539248-64539770	HepG2	liver:	n/a	n/a
18	RUNX3	chr11:64539263-64540569	GM12878	blood:	n/a	n/a
19	POLR2A	chr11:64538912-64540503	GM12878	blood:	n/a	n/a
20	POLR2A	chr11:64538790-64539805	H1-hESC	embryonic stem cell:	n/a	n/a
21	STAT3	chr11:64539583-64540453	GM12878	blood:	n/a	n/a
22	TBP	chr11:64539462-64540530	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:64534397-64541511	GM12878	blood:	n/a	n/a
24	PML	chr11:64539394-64540718	GM12878	blood:	n/a	n/a
25	POLR2A	chr11:64539257-64541496	GM12892	blood:	n/a	n/a
26	SPI1	chr11:64539323-64539724	GM12891	blood:	n/a	n/a
27	POLR2A	chr11:64539292-64539755	K562	blood:	n/a	n/a
28	ATF2	chr11:64539354-64540652	GM12878	blood:	n/a	n/a
29	SPI1	chr11:64539140-64539849	GM12878	blood:	n/a	n/a
30	POLR2A	chr11:64527091-64539806	GM12892	blood:	n/a	n/a
31	CUX1	chr11:64539181-64540263	GM12878	blood:	n/a	n/a
32	SPI1	chr11:64539330-64539803	HL-60	blood:	n/a	n/a
33	SPI1	chr11:64539359-64539720	GM12878	blood:	n/a	n/a
34	ZNF384	chr11:64539523-64540531	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:64539269-64539710	GM12892	blood:	n/a	n/a

No data

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:64510149..64512039-chr11:64538219..64540894,2	MCF-7	breast:
2	chr11:64511547..64513832-chr11:64538239..64542016,3	K562	blood:

No data

Variant related genes	Relation type
SF1	TF binding region
ENSG00000068831	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10897524	0.85[GIH][hapmap];0.88[TSI][hapmap];0.92[EUR][1000 genomes]
rs10897525	0.84[MEX][hapmap]
rs11231853	0.86[CEU][hapmap];0.82[EUR][1000 genomes]
rs11231859	1.00[CEU][hapmap];0.89[MEX][hapmap];0.82[TSI][hapmap];0.90[EUR][1000 genomes]
rs11231869	0.91[CHD][hapmap];0.90[JPT][hapmap];0.84[MEX][hapmap];0.84[ASN][1000 genomes]
rs1143937	1.00[CEU][hapmap];0.84[MEX][hapmap]
rs1207181	0.81[EUR][1000 genomes]
rs12417551	0.81[EUR][1000 genomes]
rs12575704	0.82[EUR][1000 genomes]
rs1633462	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17146121	0.89[CEU][hapmap];0.84[MEX][hapmap]
rs2003293	0.90[EUR][1000 genomes]
rs2073797	0.82[EUR][1000 genomes]
rs2073798	0.86[CHB][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.82[EUR][1000 genomes]
rs2230414	0.90[EUR][1000 genomes]
rs2267918	1.00[CEU][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.92[EUR][1000 genomes]
rs2284301	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.88[MEX][hapmap];0.88[TSI][hapmap];0.92[EUR][1000 genomes]
rs2375335	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2959652	1.00[CEU][hapmap];0.86[CHB][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.95[EUR][1000 genomes]
rs3741398	1.00[CEU][hapmap];0.86[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.90[JPT][hapmap];0.89[MEX][hapmap];0.88[TSI][hapmap];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3809076	0.89[CEU][hapmap];0.84[MEX][hapmap];0.82[TSI][hapmap];0.89[EUR][1000 genomes]
rs474707	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs476037	0.89[CEU][hapmap];0.84[MEX][hapmap]
rs477549	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.90[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.88[TSI][hapmap];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs483962	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs487105	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.95[JPT][hapmap];0.89[MEX][hapmap];0.88[TSI][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs489192	1.00[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap];0.84[MEX][hapmap];0.82[TSI][hapmap];0.80[EUR][1000 genomes]
rs490980	0.89[CEU][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs494128	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs496914	1.00[CEU][hapmap];0.94[MEX][hapmap];0.88[TSI][hapmap];0.92[EUR][1000 genomes]
rs523200	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs523752	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs532747	0.85[GIH][hapmap];0.84[MEX][hapmap];0.80[EUR][1000 genomes]
rs547066	0.83[MEX][hapmap]
rs555974	0.82[EUR][1000 genomes]
rs569602	0.86[CHB][hapmap];0.85[GIH][hapmap];0.84[MEX][hapmap];0.80[EUR][1000 genomes]
rs580374	0.92[EUR][1000 genomes]
rs58483071	0.90[EUR][1000 genomes]
rs589691	1.00[CEU][hapmap];0.85[CHB][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs593394	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs606458	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];0.90[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs607389	1.00[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs620006	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs624975	0.90[CEU][hapmap];0.84[MEX][hapmap]
rs625172	0.86[CHB][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.82[EUR][1000 genomes]
rs630966	0.82[EUR][1000 genomes]
rs633923	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs637332	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs667237	0.90[EUR][1000 genomes]
rs669976	0.90[CEU][hapmap];0.84[MEX][hapmap]
rs674297	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs677298	1.00[CEU][hapmap]
rs683841	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs684720	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs693235	0.90[CEU][hapmap];0.94[MEX][hapmap];0.88[TSI][hapmap]
rs72643567	0.84[EUR][1000 genomes]
rs72643568	0.84[EUR][1000 genomes]
rs7938455	0.80[EUR][1000 genomes]
rs7939965	0.89[CEU][hapmap];0.84[MEX][hapmap];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897694	chr11:64334114-64584959	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv818842	chr11:64345448-64546391	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
3	nsv528506	chr11:64345448-64701030	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
4	nsv555196	chr11:64357072-64559898	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
5	nsv897695	chr11:64357072-64701030	Weak transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
6	nsv555198	chr11:64373899-64573589	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
7	nsv897697	chr11:64447420-64584959	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
8	nsv897698	chr11:64447420-64621573	Active TSS Bivalent Enhancer Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription 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 target site	82 gene(s)	inside rSNPs	diseases
9	nsv897699	chr11:64447420-64638041	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
10	nsv897700	chr11:64447420-64701030	Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' 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	1071 gene(s)	inside rSNPs	diseases
11	nsv555202	chr11:64477050-64573589	Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
12	nsv468597	chr11:64477050-64584959	Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv468598	chr11:64477050-64584959	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
14	nsv555203	chr11:64477050-64584959	Strong transcription Genic enhancers Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
15	nsv1049744	chr11:64486615-64630149	Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
16	nsv832189	chr11:64487183-64620199	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
17	nsv469962	chr11:64527080-64621573	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
18	nsv897702	chr11:64532579-64584231	Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
19	nsv825947	chr11:64538092-64550927	Active TSS Flanking Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
20	nsv897703	chr11:64538346-64574200	Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs680273	PYGM	cis	cerebellum	SCAN
rs680273	EHD1	cis	cerebellum	SCAN
rs680273	ANKRD13D	cis	parietal	SCAN
rs680273	PYGM	cis	parietal	SCAN
rs680273	B3GNT1	cis	cerebellum	SCAN
rs680273	SF1	Cis_1M	lymphoblastoid	RTeQTL
rs680273	SF1	cis	lymphoblastoid	seeQTL
rs680273	TMEM138	cis	parietal	SCAN
rs680273	POLA2	cis	cerebellum	SCAN
rs680273	LRRN4CL	cis	cerebellum	SCAN
rs680273	CABP2	cis	parietal	SCAN
rs680273	TMEM138	cis	cerebellum	SCAN
rs680273	MALAT1	cis	parietal	SCAN
rs680273	SF1	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64528200-64543600	Strong transcription	Fetal Intestine Small	intestine
2	chr11:64529600-64543200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr11:64529800-64543200	Strong transcription	Fetal Brain Female	brain
4	chr11:64529800-64543600	Strong transcription	Fetal Lung	lung
5	chr11:64529800-64543600	Strong transcription	Rectal Mucosa Donor 31	rectum
6	chr11:64530000-64541200	Strong transcription	Aorta	Aorta
7	chr11:64530000-64543400	Strong transcription	Fetal Intestine Large	intestine
8	chr11:64530200-64540200	Strong transcription	Sigmoid Colon	Sigmoid Colon
9	chr11:64530400-64543000	Strong transcription	Hela-S3	cervix
10	chr11:64530400-64544200	Strong transcription	Placenta Amnion	Placenta Amnion
11	chr11:64530600-64544400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:64531400-64542600	Strong transcription	Gastric	stomach
13	chr11:64531400-64543600	Strong transcription	NHDF-Ad	bronchial
14	chr11:64531600-64540400	Strong transcription	HepG2	liver
15	chr11:64531600-64542800	Strong transcription	K562	blood
16	chr11:64531800-64540400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr11:64531800-64541000	Strong transcription	Small Intestine	intestine
18	chr11:64532000-64539800	Strong transcription	Stomach Mucosa	stomach
19	chr11:64532000-64542800	Strong transcription	Brain Germinal Matrix	brain
20	chr11:64532000-64543000	Weak transcription	Right Atrium	heart
21	chr11:64532000-64543600	Strong transcription	HSMM	muscle
22	chr11:64532000-64543800	Strong transcription	Osteobl	bone
23	chr11:64532000-64544000	Strong transcription	Colonic Mucosa	Colon
24	chr11:64532000-64544000	Strong transcription	Fetal Stomach	stomach
25	chr11:64532200-64540200	Strong transcription	Ovary	ovary
26	chr11:64532400-64543400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:64532400-64543600	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr11:64532400-64543600	Strong transcription	NH-A	brain
29	chr11:64532400-64543800	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr11:64532400-64544000	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr11:64532600-64540200	Strong transcription	Fetal Muscle Leg	muscle
32	chr11:64532600-64540400	Strong transcription	NHLF	lung
33	chr11:64532600-64543600	Genic enhancers	Primary T cells fromperipheralblood	blood
34	chr11:64532600-64544200	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr11:64532600-64544400	Strong transcription	Fetal Muscle Trunk	muscle
36	chr11:64532800-64539800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr11:64532800-64540200	Strong transcription	Duodenum Mucosa	Duodenum
38	chr11:64532800-64540200	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr11:64532800-64543600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
40	chr11:64532800-64543600	Strong transcription	NHEK	skin
41	chr11:64532800-64543800	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr11:64532800-64544200	Strong transcription	H9 Cell Line	embryonic stem cell
43	chr11:64533000-64540000	Genic enhancers	Primary T cells from cord blood	blood
44	chr11:64533000-64541200	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr11:64533000-64541800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:64533000-64543000	Strong transcription	Right Ventricle	heart
47	chr11:64533200-64540800	Strong transcription	HMEC	breast
48	chr11:64533200-64541800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr11:64533200-64541800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr11:64533200-64543600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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