Variant report

Variant	rs12223914
Chromosome Location	chr11:64511886-64511887
allele	G/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	HDAC2	chr11:64511885-64512109	K562	blood:	n/a	n/a
2	RUNX3	chr11:64511780-64512048	GM12878	blood:	n/a	n/a
3	RAD21	chr11:64510133-64512065	SK-N-SH	brain:	n/a	chr11:64511012-64511025 chr11:64510945-64510958 chr11:64511205-64511217 chr11:64511203-64511222 chr11:64512029-64512041
4	MAZ	chr11:64509811-64513853	K562	blood:	n/a	chr11:64512748-64512757 chr11:64512445-64512454 chr11:64512631-64512641 chr11:64510447-64510457 chr11:64513619-64513629 chr11:64513719-64513729
5	POLR2A	chr11:64511016-64511967	K562	blood:	n/a	n/a
6	ZBTB7A	chr11:64511805-64513945	K562	blood:	n/a	chr11:64512696-64512703
7	CTCF	chr11:64511760-64511910	NHLF	lung:	n/a	n/a
8	MAX	chr11:64511049-64512031	NB4	blood:	n/a	n/a
9	MAX	chr11:64509884-64513844	K562	blood:	n/a	chr11:64512748-64512757 chr11:64512445-64512454 chr11:64512631-64512641 chr11:64510447-64510457 chr11:64513619-64513629 chr11:64513719-64513729
10	MYC	chr11:64510352-64511985	K562	blood:	n/a	chr11:64510447-64510457
11	POLR2A	chr11:64511045-64513691	Raji	blood:	n/a	n/a
12	RUNX3	chr11:64511084-64511887	GM12878	blood:	n/a	n/a
13	YY1	chr11:64511851-64512038	K562	blood:	n/a	n/a
14	MTA3	chr11:64511069-64512036	GM12878	blood:	n/a	n/a
15	EGR1	chr11:64511877-64512297	GM12878	blood:	n/a	chr11:64512168-64512178 chr11:64512113-64512127 chr11:64512068-64512082
16	CTCF	chr11:64511760-64511910	SAEC	small airway:	n/a	n/a
17	POLR2A	chr11:64508984-64513948	HL-60	blood:	n/a	n/a
18	RCOR1	chr11:64511807-64512067	K562	blood:	n/a	n/a
19	RCOR1	chr11:64509845-64512147	K562	blood:	n/a	n/a
20	MAX	chr11:64509967-64512087	A549	lung:	n/a	chr11:64510447-64510457
21	ZBTB7A	chr11:64511709-64511985	K562	blood:	n/a	n/a
22	BACH1	chr11:64511055-64512010	H1-hESC	embryonic stem cell:	n/a	n/a
23	MXI1	chr11:64511078-64514070	SK-N-SH	brain:	n/a	n/a
24	ESRRA	chr11:64509625-64512230	GM12878	blood:	n/a	chr11:64511737-64511750
25	POLR2A	chr11:64510220-64513732	NB4	blood:	n/a	n/a
26	CTCF	chr11:64509969-64512104	SK-N-SH	brain:	n/a	chr11:64511203-64511219 chr11:64510949-64510958 chr11:64510690-64510703 chr11:64511985-64511998 chr11:64511202-64511220 chr11:64511205-64511218 chr11:64510494-64510504 chr11:64510492-64510508 chr11:64510491-64510509 chr11:64510946-64510959 chr11:64511205-64511218 chr11:64510497-64510506
27	RCOR1	chr11:64511884-64511977	Hela-S3	cervix:	n/a	n/a
28	ZBTB7A	chr11:64510226-64512265	ECC-1	luminal epithelium:	n/a	chr11:64510902-64510911
29	MYC	chr11:64509954-64513563	NB4	blood:	n/a	chr11:64512748-64512757 chr11:64512445-64512454 chr11:64512631-64512641 chr11:64510447-64510457
30	JUN	chr11:64509522-64512102	K562	blood:	n/a	chr11:64510482-64510491 chr11:64509927-64509936
31	TEAD4	chr11:64510316-64511987	K562	blood:	n/a	n/a
32	ZNF143	chr11:64511791-64512076	K562	blood:	n/a	n/a
33	EGR1	chr11:64511435-64513920	K562	blood:	n/a	chr11:64513281-64513294 chr11:64513276-64513298 chr11:64512704-64512714 chr11:64513281-64513294 chr11:64512415-64512425 chr11:64512960-64512973 chr11:64511680-64511693 chr11:64513280-64513294 chr11:64512559-64512569 chr11:64513717-64513727 chr11:64513282-64513291 chr11:64513281-64513294 chr11:64512168-64512178 chr11:64513282-64513293 chr11:64513615-64513628 chr11:64513278-64513292 chr11:64513620-64513630 chr11:64512113-64512127 chr11:64513282-64513292 chr11:64513613-64513623 chr11:64511708-64511718 chr11:64513719-64513729 chr11:64513719-64513732 chr11:64513280-64513295 chr11:64513281-64513294 chr11:64512632-64512642 chr11:64512068-64512082 chr11:64512965-64512975 chr11:64513282-64513292 chr11:64513732-64513745 chr11:64513732-64513742
34	CTCF	chr11:64510001-64512103	A549	lung:	n/a	chr11:64511203-64511219 chr11:64510949-64510958 chr11:64510690-64510703 chr11:64511985-64511998 chr11:64511202-64511220 chr11:64511205-64511218 chr11:64510494-64510504 chr11:64510492-64510508 chr11:64510491-64510509 chr11:64510946-64510959 chr11:64511205-64511218 chr11:64510497-64510506
35	POLR2A	chr11:64511874-64513726	K562	blood:	n/a	n/a
36	MAZ	chr11:64511050-64513713	GM12878	blood:	n/a	chr11:64512748-64512757 chr11:64512445-64512454 chr11:64512631-64512641 chr11:64513619-64513629
37	POLR2A	chr11:64510046-64513744	HL-60	blood:	n/a	n/a
38	MXI1	chr11:64511307-64511888	IMR90	lung:	n/a	n/a
39	CBX3	chr11:64510875-64512128	K562	blood:	n/a	n/a
40	EGR1	chr11:64511841-64512598	K562	blood:	n/a	chr11:64512415-64512425 chr11:64512559-64512569 chr11:64512168-64512178 chr11:64512113-64512127 chr11:64512068-64512082
41	ZBTB7A	chr11:64510228-64512262	ECC-1	luminal epithelium:	n/a	chr11:64510902-64510911
42	POLR2A	chr11:64510013-64512330	K562	blood:	n/a	n/a
43	ELF1	chr11:64510971-64512097	GM12878	blood:	n/a	chr11:64511000-64511012 chr11:64511157-64511169 chr11:64512029-64512041 chr11:64511099-64511111 chr11:64511715-64511727

No.	Distal block	Cell Line	Cell type
1	chr11:64511547..64513832-chr11:64538239..64542016,3	K562	blood:
2	chr11:64507790..64516181-chr11:64524582..64537783,30	K562	blood:
3	chr11:64510149..64512039-chr11:64538219..64540894,2	MCF-7	breast:
4	chr11:64506030..64508610-chr11:64510560..64513523,3	MCF-7	breast:
5	chr11:64489351..64492621-chr11:64507509..64512935,5	K562	blood:
6	chr11:64124497..64126994-chr11:64509396..64512374,2	K562	blood:
7	chr11:64509857..64513722-chr11:64571129..64574033,3	MCF-7	breast:
8	chr11:64509755..64511903-chr11:65684738..65686627,2	K562	blood:
9	chr11:64510354..64515027-chr11:64543156..64548358,11	K562	blood:

Variant related genes	Relation type
RASGRP2	TF binding region
ENSG00000168066	Chromatin interaction
ENSG00000133895	Chromatin interaction
ENSG00000175573	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000068831	Chromatin interaction
ENSG00000068976	Chromatin interaction
ENSG00000110076	Chromatin interaction
ENSG00000269038	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10897524	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10897525	0.81[AMR][1000 genomes]
rs11231859	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1207113	0.91[ASN][1000 genomes]
rs1207181	0.91[ASN][1000 genomes]
rs1633462	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2003293	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2073797	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2073798	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2230414	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2267918	0.86[EUR][1000 genomes]
rs2284301	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2375335	0.83[EUR][1000 genomes]
rs2959652	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3741398	0.83[AMR][1000 genomes]
rs3809076	0.83[EUR][1000 genomes]
rs474707	0.81[EUR][1000 genomes]
rs477549	0.83[EUR][1000 genomes]
rs483962	0.85[EUR][1000 genomes]
rs487105	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs489192	0.80[ASN][1000 genomes]
rs494128	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs496914	0.86[EUR][1000 genomes]
rs523200	0.82[EUR][1000 genomes]
rs532747	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs547066	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs555974	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs569602	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs580374	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58483071	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs589691	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs593394	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs620006	0.82[EUR][1000 genomes]
rs625172	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs630966	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs633923	0.81[EUR][1000 genomes]
rs637332	0.85[EUR][1000 genomes]
rs667237	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs673224	0.80[EUR][1000 genomes]
rs674297	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs677298	0.80[AMR][1000 genomes]
rs684720	0.82[AMR][1000 genomes]
rs686171	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72643567	0.82[EUR][1000 genomes]
rs72643568	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7938455	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv468596	chr11:64334114-64527080	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer Flanking 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	28 gene(s)	inside rSNPs	diseases
2	nsv555195	chr11:64334114-64527080	Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	nsv897701	chr11:64501991-64520569	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs12223914	SF1	Cis_1M	lymphoblastoid	RTeQTL
rs12223914	SF1	cis	multi-tissue	Pritchard

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64508600-64513000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
2	chr11:64508800-64512000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr11:64509000-64512000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
4	chr11:64509200-64512000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:64509200-64512000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
6	chr11:64509200-64512600	Active TSS	Brain Anterior Caudate	brain
7	chr11:64509400-64512000	Flanking Active TSS	Primary B cells from cord blood	blood
8	chr11:64509400-64512000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
9	chr11:64509400-64512000	Flanking Active TSS	Right Ventricle	heart
10	chr11:64509400-64512000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr11:64509400-64512200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:64509400-64513600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
13	chr11:64509600-64512000	Flanking Active TSS	Primary hematopoietic stem cells	blood
14	chr11:64509600-64512000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr11:64509600-64512000	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
16	chr11:64509600-64512000	Flanking Active TSS	Spleen	Spleen
17	chr11:64509600-64512200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
18	chr11:64509600-64512400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr11:64509600-64512600	Enhancers	Fetal Heart	heart
20	chr11:64509600-64513600	Active TSS	Left Ventricle	heart
21	chr11:64509800-64512000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
22	chr11:64509800-64513200	Active TSS	Primary T killer memory cells from peripheral blood	blood
23	chr11:64509800-64513600	Active TSS	Right Atrium	heart
24	chr11:64509800-64514000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
25	chr11:64510000-64512000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
26	chr11:64510000-64512200	Flanking Active TSS	Thymus	Thymus
27	chr11:64510000-64513400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
28	chr11:64510000-64513400	Active TSS	Aorta	Aorta
29	chr11:64510000-64513600	Active TSS	Primary T cells from cord blood	blood
30	chr11:64510200-64513400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:64510200-64513400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
32	chr11:64510400-64512000	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
33	chr11:64510400-64512000	Bivalent Enhancer	HUVEC	blood vessel
34	chr11:64510400-64512800	Active TSS	Primary B cells from peripheral blood	blood
35	chr11:64510400-64513400	Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr11:64510400-64513400	Active TSS	Brain Angular Gyrus	brain
37	chr11:64510600-64512000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr11:64510600-64512000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
39	chr11:64510600-64512000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
40	chr11:64510600-64512000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
41	chr11:64510600-64512000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
42	chr11:64510600-64512000	Flanking Active TSS	Liver	Liver
43	chr11:64510600-64512000	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
44	chr11:64510600-64512000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
45	chr11:64510600-64512000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
46	chr11:64510600-64512000	Flanking Bivalent TSS/Enh	HepG2	liver
47	chr11:64510600-64512200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr11:64510600-64512200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
49	chr11:64510800-64512000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr11:64510800-64512000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood

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