Variant report

Variant	rs523200
Chromosome Location	chr11:64532579-64532580
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:40)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:40 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:64532364-64532747	SK-N-SH	brain:	n/a	n/a
2	POLR2A	chr11:64526696-64538505	K562	blood:	n/a	n/a
3	POLR2A	chr11:64532079-64532736	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr11:64525013-64542071	HepG2	liver:	n/a	n/a
5	POLR2A	chr11:64528801-64539251	GM12892	blood:	n/a	n/a
6	POLR2A	chr11:64529075-64533137	GM12891	blood:	n/a	n/a
7	POLR2A	chr11:64527305-64538579	K562	blood:	n/a	n/a
8	POLR2A	chr11:64528860-64533465	PFSK-1	brain:	n/a	n/a
9	POLR2A	chr11:64528964-64532627	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr11:64532274-64532689	MCF-7	breast:	n/a	n/a
11	POLR2A	chr11:64532052-64532780	K562	blood:	n/a	n/a
12	POLR2A	chr11:64525521-64533450	A549	lung:	n/a	n/a
13	POLR2A	chr11:64532274-64532656	GM12878	blood:	n/a	n/a
14	POLR2A	chr11:64528977-64538125	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr11:64527082-64533748	GM12878	blood:	n/a	n/a
16	CTCF	chr11:64532519-64533407	A549	lung:	n/a	n/a
17	POLR2A	chr11:64529490-64533356	GM12878	blood:	n/a	n/a
18	POLR2A	chr11:64529491-64532624	GM12891	blood:	n/a	n/a
19	CTCF	chr11:64532520-64532670	GM12874	blood:	n/a	n/a
20	POLR2A	chr11:64527460-64534329	GM12892	blood:	n/a	n/a
21	POLR2A	chr11:64529649-64532669	GM12878	blood:	n/a	n/a
22	POLR2A	chr11:64526410-64533727	GM12891	blood:	n/a	n/a
23	POLR2A	chr11:64532238-64533225	PFSK-1	brain:	n/a	n/a
24	POLR2A	chr11:64526666-64533511	SK-N-MC	brain:	n/a	n/a
25	POLR2A	chr11:64532111-64532674	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr11:64532416-64532853	U87	brain:	n/a	n/a
27	POLR2A	chr11:64532132-64532775	HepG2	liver:	n/a	n/a
28	POLR2A	chr11:64529493-64533360	GM12891	blood:	n/a	n/a
29	USF2	chr11:64532535-64533195	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr11:64532223-64532682	K562	blood:	n/a	n/a
31	POLR2A	chr11:64526699-64532799	PANC-1	pancreas:	n/a	n/a
32	POLR2A	chr11:64529558-64533705	K562	blood:	n/a	n/a
33	POLR2A	chr11:64529494-64533360	GM12892	blood:	n/a	n/a
34	POLR2A	chr11:64527091-64539806	GM12892	blood:	n/a	n/a
35	POLR2A	chr11:64532163-64532720	HL-60	blood:	n/a	n/a
36	POLR2A	chr11:64529560-64533358	K562	blood:	n/a	n/a
37	POLR2A	chr11:64529570-64533197	HL-60	blood:	n/a	n/a
38	POLR2A	chr11:64532315-64533225	U87	brain:	n/a	n/a
39	POLR2A	chr11:64532547-64532744	HCT-116	colon:	n/a	n/a
40	POLR2A	chr11:64532160-64533213	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:64529809..64532784-chr22:39706393..39708721,2	K562	blood:
2	chr11:64507790..64516181-chr11:64524582..64537783,30	K562	blood:

No data

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

Extended variants
information (count: 83 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10400348	0.81[EUR][1000 genomes]
rs10792444	0.82[EUR][1000 genomes]
rs10897524	0.88[TSI][hapmap];0.95[EUR][1000 genomes]
rs10897525	0.84[MEX][hapmap]
rs11231853	0.86[CEU][hapmap];0.86[EUR][1000 genomes]
rs11231859	1.00[CEU][hapmap];0.89[MEX][hapmap];0.82[TSI][hapmap];0.93[EUR][1000 genomes]
rs11231869	0.91[CHD][hapmap];0.90[GIH][hapmap];0.90[JPT][hapmap];0.84[MEX][hapmap];0.84[ASN][1000 genomes]
rs1143937	1.00[CEU][hapmap];0.86[GIH][hapmap];0.84[MEX][hapmap]
rs1207181	0.84[EUR][1000 genomes]
rs12223914	0.82[EUR][1000 genomes]
rs12417551	0.84[EUR][1000 genomes]
rs12575704	0.86[EUR][1000 genomes]
rs1633462	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17146121	0.89[CEU][hapmap];0.84[MEX][hapmap]
rs2003293	0.93[EUR][1000 genomes]
rs2073797	0.85[EUR][1000 genomes]
rs2073798	0.86[CHB][hapmap];0.86[GIH][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.85[EUR][1000 genomes]
rs2230414	0.93[EUR][1000 genomes]
rs2267918	1.00[CEU][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.95[EUR][1000 genomes]
rs2284301	1.00[CEU][hapmap];0.81[CHB][hapmap];0.88[MEX][hapmap];0.88[TSI][hapmap];0.95[EUR][1000 genomes]
rs2375335	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2959652	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[GIH][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.98[EUR][1000 genomes]
rs3741398	1.00[CEU][hapmap];0.86[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.89[MEX][hapmap];0.88[TSI][hapmap];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3809076	0.89[CEU][hapmap];0.84[MEX][hapmap];0.82[TSI][hapmap];0.92[EUR][1000 genomes]
rs474707	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.93[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];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.88[TSI][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs483962	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs487105	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.89[MEX][hapmap];0.88[TSI][hapmap];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs489192	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[GIH][hapmap];0.85[JPT][hapmap];0.84[MEX][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs490980	0.89[CEU][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs494128	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs496914	1.00[CEU][hapmap];0.94[MEX][hapmap];0.88[TSI][hapmap];0.95[EUR][1000 genomes]
rs523752	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs532747	0.84[MEX][hapmap];0.83[EUR][1000 genomes]
rs547066	0.85[GIH][hapmap];0.83[MEX][hapmap];0.82[EUR][1000 genomes]
rs555974	0.85[EUR][1000 genomes]
rs569602	0.86[CHB][hapmap];0.84[MEX][hapmap];0.83[EUR][1000 genomes]
rs580374	0.95[EUR][1000 genomes]
rs58483071	0.93[EUR][1000 genomes]
rs589691	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[GIH][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs593394	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs606458	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs607389	1.00[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs620006	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs624975	0.90[CEU][hapmap];0.82[GIH][hapmap];0.84[MEX][hapmap]
rs625172	0.86[CHB][hapmap];0.86[GIH][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.85[EUR][1000 genomes]
rs630966	0.85[EUR][1000 genomes]
rs633923	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs637332	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs667237	0.93[EUR][1000 genomes]
rs669976	0.90[CEU][hapmap];0.86[GIH][hapmap];0.84[MEX][hapmap]
rs674297	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs677298	1.00[CEU][hapmap]
rs680273	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]
rs683841	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs684720	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs686171	0.82[EUR][1000 genomes]
rs693235	0.90[CEU][hapmap];0.94[MEX][hapmap];0.88[TSI][hapmap]
rs72643567	0.87[EUR][1000 genomes]
rs72643568	0.87[EUR][1000 genomes]
rs7938455	0.83[EUR][1000 genomes]
rs7939965	0.89[CEU][hapmap];0.84[MEX][hapmap];0.86[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	nsv1051350	chr11:64372906-64533632	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	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
8	esv1804443	chr11:64386453-64534785	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh 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	33 gene(s)	inside rSNPs	diseases
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs523200	B3GNT1	cis	cerebellum	SCAN
rs523200	SF1	Cis_1M	lymphoblastoid	RTeQTL
rs523200	LRRN4CL	cis	cerebellum	SCAN
rs523200	CABP2	cis	parietal	SCAN
rs523200	PYGM	cis	parietal	SCAN
rs523200	TMEM138	cis	parietal	SCAN
rs523200	SF1	cis	lymphoblastoid	seeQTL
rs523200	SF1	cis	multi-tissue	Pritchard
rs523200	MALAT1	cis	parietal	SCAN
rs523200	PYGM	cis	cerebellum	SCAN
rs523200	ANKRD13D	cis	parietal	SCAN
rs523200	EHD1	cis	cerebellum	SCAN
rs523200	POLA2	cis	cerebellum	SCAN
rs523200	TMEM138	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64525400-64533400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:64527400-64539600	Genic enhancers	Primary B cells from peripheral blood	blood
3	chr11:64527600-64534600	Weak transcription	Fetal Brain Male	brain
4	chr11:64528000-64532600	Genic enhancers	Fetal Muscle Trunk	muscle
5	chr11:64528000-64532600	Genic enhancers	Fetal Muscle Leg	muscle
6	chr11:64528000-64536400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr11:64528200-64533400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:64528200-64543600	Strong transcription	Fetal Intestine Small	intestine
9	chr11:64529000-64533400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr11:64529400-64532600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr11:64529400-64532600	Genic enhancers	Spleen	Spleen
12	chr11:64529600-64532800	Genic enhancers	NHEK	skin
13	chr11:64529600-64533000	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
14	chr11:64529600-64533200	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:64529600-64533600	Genic enhancers	Primary hematopoietic stem cells	blood
16	chr11:64529600-64534800	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:64529600-64543200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr11:64529800-64532600	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
19	chr11:64529800-64532600	Genic enhancers	HUVEC	blood vessel
20	chr11:64529800-64532800	Genic enhancers	Duodenum Smooth Muscle	Duodenum
21	chr11:64529800-64532800	Genic enhancers	Rectal Mucosa Donor 29	rectum
22	chr11:64529800-64532800	Genic enhancers	A549	lung
23	chr11:64529800-64533000	Genic enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:64529800-64533000	Genic enhancers	Left Ventricle	heart
25	chr11:64529800-64533000	Genic enhancers	Right Ventricle	heart
26	chr11:64529800-64533200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr11:64529800-64533200	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr11:64529800-64533200	Enhancers	Fetal Heart	heart
29	chr11:64529800-64533200	Genic enhancers	HMEC	breast
30	chr11:64529800-64533400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr11:64529800-64534000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:64529800-64536000	Genic enhancers	Fetal Thymus	thymus
33	chr11:64529800-64537800	Genic enhancers	Dnd41	blood
34	chr11:64529800-64539400	Strong transcription	Liver	Liver
35	chr11:64529800-64543200	Strong transcription	Fetal Brain Female	brain
36	chr11:64529800-64543600	Strong transcription	Fetal Lung	lung
37	chr11:64529800-64543600	Strong transcription	Rectal Mucosa Donor 31	rectum
38	chr11:64530000-64534200	Genic enhancers	Thymus	Thymus
39	chr11:64530000-64541200	Strong transcription	Aorta	Aorta
40	chr11:64530000-64543400	Strong transcription	Fetal Intestine Large	intestine
41	chr11:64530200-64532600	Genic enhancers	NHLF	lung
42	chr11:64530200-64533200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr11:64530200-64533400	Genic enhancers	GM12878-XiMat	blood
44	chr11:64530200-64534600	Strong transcription	Lung	lung
45	chr11:64530200-64540200	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr11:64530400-64532800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr11:64530400-64532800	Genic enhancers	Duodenum Mucosa	Duodenum
48	chr11:64530400-64533000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
49	chr11:64530400-64533200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr11:64530400-64543000	Strong transcription	Hela-S3	cervix

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