Variant report

Variant	rs550015
Chromosome Location	chr11:65186348-65186349
allele	A/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	YY1	chr11:65186325-65186892	SK-N-SH_RA	brain:	n/a	chr11:65186805-65186813
2	CREB1	chr11:65185741-65186950	A549	lung:	n/a	n/a
3	USF2	chr11:65186022-65186787	H1-hESC	embryonic stem cell:	n/a	chr11:65186307-65186316 chr11:65186305-65186318 chr11:65186577-65186590 chr11:65186306-65186315 chr11:65186308-65186317 chr11:65186307-65186316 chr11:65186305-65186316
4	KAP1	chr11:65186100-65186917	HEK293	kidney:	n/a	n/a
5	SP1	chr11:65186057-65186873	GM12878	blood:	n/a	chr11:65186641-65186650 chr11:65186640-65186650 chr11:65186639-65186651 chr11:65186154-65186168 chr11:65186639-65186651 chr11:65186636-65186650 chr11:65186640-65186649 chr11:65186640-65186650
6	RELA	chr11:65185958-65187214	GM18951	blood:	n/a	chr11:65186981-65186990 chr11:65186981-65186990
7	CHD1	chr11:65183014-65218224	IMR90	lung:	n/a	chr11:65189696-65189706 chr11:65213009-65213016
8	SPI1	chr11:65185883-65186450	GM12891	blood:	n/a	chr11:65186091-65186100 chr11:65185910-65185923
9	TEAD4	chr11:65185940-65186857	HepG2	liver:	n/a	n/a
10	MYC	chr11:65186127-65186722	MCF10A-Er-Src	breast:	n/a	chr11:65186307-65186316 chr11:65186579-65186588
11	REST	chr11:65186062-65186454	Hela-S3	cervix:	n/a	chr11:65186135-65186144 chr11:65186123-65186136
12	ETS1	chr11:65185974-65187071	K562	blood:	n/a	chr11:65186983-65186992 chr11:65186084-65186097
13	ESR1	chr11:65185959-65186828	ECC-1	luminal epithelium:	n/a	chr11:65185972-65185989 chr11:65186272-65186287
14	RCOR1	chr11:65185945-65186996	HepG2	liver:	n/a	n/a
15	HNF4A	chr11:65186059-65186526	HepG2	liver:	n/a	n/a
16	MYC	chr11:65186056-65186824	HepG2	liver:	n/a	chr11:65186307-65186316 chr11:65186579-65186588
17	HA-E2F1	chr11:65186023-65186966	MCF-7	breast:	n/a	n/a
18	RAD21	chr11:65186100-65186785	HepG2	liver:	n/a	n/a
19	TCF7L2	chr11:65186145-65186746	HepG2	liver:	n/a	n/a
20	YY1	chr11:65186034-65186974	ECC-1	luminal epithelium:	n/a	chr11:65186805-65186813
21	ZNF217	chr11:65186003-65186732	MCF-7	breast:	n/a	n/a
22	MAFF	chr11:65186114-65186983	K562	blood:	n/a	n/a
23	ETS1	chr11:65185880-65186909	A549	lung:	n/a	chr11:65186084-65186097
24	EBF1	chr11:65185878-65186887	GM12878	blood:	n/a	n/a
25	ELK1	chr11:65186265-65186649	K562	blood:	n/a	n/a
26	TEAD4	chr11:65185954-65186968	K562	blood:	n/a	n/a
27	TAF1	chr11:65186001-65187000	H1-hESC	embryonic stem cell:	n/a	n/a
28	MYC	chr11:65186094-65186618	MCF-7	breast:	n/a	chr11:65186307-65186316 chr11:65186579-65186588
29	SP1	chr11:65185958-65186919	HepG2	liver:	n/a	chr11:65186641-65186650 chr11:65186640-65186650 chr11:65186639-65186651 chr11:65186154-65186168 chr11:65186639-65186651 chr11:65186636-65186650 chr11:65186640-65186649 chr11:65186640-65186650
30	ZNF143	chr11:65186103-65186807	K562	blood:	n/a	n/a
31	POLR2A	chr11:65185908-65188050	HUVEC	blood vessel:	n/a	n/a
32	EP300	chr11:65186109-65186965	GM12878	blood:	n/a	n/a
33	POLR2A	chr11:65182982-65199920	Hela-S3	cervix:	n/a	n/a
34	FOXA1	chr11:65186054-65186518	T-47D	breast:	n/a	n/a
35	MYC	chr11:65186079-65186912	K562	blood:	n/a	chr11:65186307-65186316 chr11:65186579-65186588
36	GABPA	chr11:65185942-65186970	K562	blood:	n/a	n/a
37	SP1	chr11:65185725-65187934	A549	lung:	n/a	chr11:65186641-65186650 chr11:65186640-65186650 chr11:65186639-65186651 chr11:65186154-65186168 chr11:65186639-65186651 chr11:65185857-65185871 chr11:65186636-65186650 chr11:65185861-65185870 chr11:65186640-65186649 chr11:65185861-65185871 chr11:65185910-65185924 chr11:65186640-65186650
38	TAF7	chr11:65186057-65186895	H1-hESC	embryonic stem cell:	n/a	n/a
39	NR2F2	chr11:65185235-65188013	K562	blood:	n/a	chr11:65186278-65186293
40	TFAP2C	chr11:65185329-65187138	Hela-S3	cervix:	n/a	chr11:65185967-65185982
41	TAF1	chr11:65185972-65187163	A549	lung:	n/a	n/a
42	GATA3	chr11:65185734-65186882	MCF-7	breast:	n/a	n/a
43	SP1	chr11:65186083-65186947	H1-hESC	embryonic stem cell:	n/a	chr11:65186641-65186650 chr11:65186640-65186650 chr11:65186639-65186651 chr11:65186154-65186168 chr11:65186639-65186651 chr11:65186636-65186650 chr11:65186640-65186649 chr11:65186640-65186650
44	YY1	chr11:65186047-65186967	K562	blood:	n/a	chr11:65186805-65186813
45	RFX5	chr11:65186060-65186910	Hela-S3	cervix:	n/a	chr11:65186571-65186586
46	JUND	chr11:65185657-65186929	K562	blood:	n/a	n/a
47	YY1	chr11:65185969-65187087	GM12878	blood:	n/a	chr11:65186805-65186813
48	POLR2A	chr11:65185765-65189757	GM12892	blood:	n/a	n/a
49	MEF2A	chr11:65186053-65186776	K562	blood:	n/a	n/a
50	POLR2A	chr11:65184755-65189855	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65058175..65060468-chr11:65184473..65187449,2	MCF-7	breast:
2	chr11:65186188..65187145-chr5:34914760..34915691,2	Hela-S3	cervix:
3	chr11:65185954..65186504-chr17:80186339..80187075,2	Hela-S3	cervix:
4	chr11:65095990..65098961-chr11:65184983..65186662,2	K562	blood:
5	chr11:65186118..65186781-chr11:65225762..65226605,2	MCF-7	breast:
6	chr11:65186177..65186862-chr12:115121835..115122638,2	Hela-S3	cervix:
7	chr11:65186113..65186664-chr6:159291136..159291690,2	Hela-S3	cervix:
8	chr11:65185629..65187534-chr11:65343054..65345463,3	MCF-7	breast:
9	chr11:65185609..65187437-chr2:233242948..233244448,2	MCF-7	breast:
10	chr11:65186095..65189808-chr11:65319853..65322686,3	MCF-7	breast:
11	chr11:65185895..65186454-chr5:179247747..179248389,2	Hela-S3	cervix:
12	chr1:236958219..236959023-chr11:65185969..65186737,2	Hela-S3	cervix:
13	chr11:65186294..65191468-chr11:65379126..65384544,8	MCF-7	breast:
14	chr11:65185377..65188145-chr9:37488495..37490898,2	K562	blood:
15	chr11:65178877..65218546-chr11:65218612..65286191,1014	K562	blood:
16	chr11:65183635..65190622-chr11:65305653..65310980,8	MCF-7	breast:
17	chr11:65184392..65191686-chr11:65339528..65345365,10	K562	blood:
18	chr11:65147535..65148091-chr11:65186090..65186757,2	MCF-7	breast:
19	chr11:65185509..65187331-chr11:65681398..65683279,2	MCF-7	breast:
20	chr11:65184042..65186636-chr11:65381188..65384073,2	K562	blood:
21	chr11:65186164..65187009-chr19:39970968..39971652,2	Hela-S3	cervix:
22	chr11:65186040..65189423-chr11:65316425..65320462,4	MCF-7	breast:
23	chr11:65147249..65148062-chr11:65185872..65186473,2	MCF-7	breast:
24	chr11:65184371..65196984-chr11:65316952..65328208,29	K562	blood:
25	chr11:65182317..65198249-chr11:65333937..65346467,45	MCF-7	breast:
26	chr11:65107573..65110262-chr11:65186195..65188738,2	MCF-7	breast:
27	chr11:65186090..65188584-chr5:68640496..68642731,2	MCF-7	breast:
28	chr11:65186193..65186711-chr18:74534414..74534968,2	Hela-S3	cervix:
29	chr11:65047940..65050656-chr11:65185638..65187863,2	MCF-7	breast:
30	chr11:65186020..65188324-chr11:66886027..66888384,2	MCF-7	breast:
31	chr11:65185186..65203592-chr11:65286522..65299399,55	K562	blood:
32	chr11:65147131..65148138-chr11:65185981..65186782,7	MCF-7	breast:
33	chr11:65185945..65193560-chr11:65336627..65344485,19	K562	blood:
34	chr11:65186172..65186838-chr9:132459452..132460332,2	Hela-S3	cervix:

Variant related genes	Relation type
NEAT1	TF binding region
ENSG00000173465	Chromatin interaction
ENSG00000173120	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000141526	Chromatin interaction
ENSG00000113460	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000173442	Chromatin interaction
ENSG00000014138	Chromatin interaction
ENSG00000116984	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000270526	Chromatin interaction
ENSG00000176973	Chromatin interaction
ENSG00000163283	Chromatin interaction
ENSG00000130856	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000203711	Chromatin interaction
ENSG00000260233	Chromatin interaction
ENSG00000168056	Chromatin interaction
ENSG00000113456	Chromatin interaction
ENSG00000230188	Chromatin interaction
ENSG00000161011	Chromatin interaction
ENSG00000173727	Chromatin interaction
ENSG00000142186	Chromatin interaction
ENSG00000133884	Chromatin interaction
ENSG00000135111	Chromatin interaction
ENSG00000105197	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11602839	1.00[CEU][hapmap];0.90[JPT][hapmap];1.00[EUR][1000 genomes]
rs11605125	0.85[CEU][hapmap]
rs2073801	1.00[CEU][hapmap];0.95[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2904976	1.00[CEU][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs475967	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs481335	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs508286	0.85[EUR][1000 genomes]
rs550894	0.82[EUR][1000 genomes]
rs580933	0.85[CEU][hapmap];0.91[EUR][1000 genomes]
rs61154080	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs666834	1.00[ASW][hapmap];1.00[CEU][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs673753	0.85[CEU][hapmap];0.93[GIH][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7940559	0.87[LWK][hapmap];0.88[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526181	chr11:64638041-65257329	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1539 gene(s)	inside rSNPs	diseases
2	esv2422285	chr11:65013294-65254540	Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	474 gene(s)	inside rSNPs	diseases
3	nsv897715	chr11:65083491-65427346	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
4	nsv897716	chr11:65083491-65481166	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS 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	999 gene(s)	inside rSNPs	diseases
5	nsv541065	chr11:65117387-65271894	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	835 gene(s)	inside rSNPs	diseases
6	esv1829999	chr11:65136686-65343124	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	963 gene(s)	inside rSNPs	diseases
7	nsv897717	chr11:65140209-65278461	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	942 gene(s)	inside rSNPs	diseases
8	nsv897718	chr11:65140209-65577516	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1003 gene(s)	inside rSNPs	diseases
9	nsv541066	chr11:65142779-65271894	Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers 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	833 gene(s)	inside rSNPs	diseases
10	nsv541067	chr11:65142779-65313799	Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	950 gene(s)	inside rSNPs	diseases
11	nsv541068	chr11:65142779-65331136	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	953 gene(s)	inside rSNPs	diseases
12	nsv541069	chr11:65142779-65368787	Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	965 gene(s)	inside rSNPs	diseases
13	nsv541070	chr11:65142779-65397058	Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription 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 miRNA target site	972 gene(s)	inside rSNPs	diseases
14	nsv541071	chr11:65142779-65429352	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
15	nsv897719	chr11:65157094-65335705	Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
16	nsv541072	chr11:65171202-65313799	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	946 gene(s)	inside rSNPs	diseases
17	nsv541073	chr11:65171202-65331136	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
18	nsv541074	chr11:65171202-65368787	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	961 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs550015	BANF1	cis	parietal	SCAN
rs550015	POLA2	cis	parietal	SCAN
rs550015	PPP6R3	cis	cerebellum	SCAN
rs550015	SLC22A25	cis	cerebellum	SCAN
rs550015	SLC22A11	cis	parietal	SCAN
rs550015	PLCB3	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65181400-65189400	Weak transcription	Ovary	ovary
2	chr11:65182200-65189600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
3	chr11:65182400-65188600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
4	chr11:65183000-65189200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:65183000-65189400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:65183200-65186800	Enhancers	Fetal Brain Male	brain
7	chr11:65183200-65186800	Enhancers	Fetal Heart	heart
8	chr11:65183200-65187200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr11:65183200-65188000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr11:65183400-65188600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr11:65183400-65188600	Flanking Active TSS	Hela-S3	cervix
12	chr11:65183400-65189200	Flanking Active TSS	Brain Anterior Caudate	brain
13	chr11:65183400-65189200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
14	chr11:65183400-65189400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
15	chr11:65183400-65189400	Flanking Active TSS	Stomach Smooth Muscle	stomach
16	chr11:65183400-65189600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
17	chr11:65183400-65189600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:65183400-65190200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr11:65183600-65186600	Enhancers	Placenta Amnion	Placenta Amnion
20	chr11:65183600-65187400	Flanking Active TSS	Rectal Smooth Muscle	rectum
21	chr11:65183600-65188000	Flanking Active TSS	Brain Cingulate Gyrus	brain
22	chr11:65183600-65188000	Flanking Active TSS	Brain Hippocampus Middle	brain
23	chr11:65183600-65188600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr11:65183600-65188600	Flanking Active TSS	Adipose Nuclei	Adipose
25	chr11:65183600-65188600	Flanking Active TSS	Colonic Mucosa	Colon
26	chr11:65183600-65188600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr11:65183600-65189000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr11:65183600-65189200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
29	chr11:65183600-65189400	Flanking Active TSS	GM12878-XiMat	blood
30	chr11:65183600-65189600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr11:65183600-65189600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
32	chr11:65183600-65189600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
33	chr11:65183600-65189600	Flanking Active TSS	Dnd41	blood
34	chr11:65183600-65189800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr11:65183600-65194200	Flanking Active TSS	Primary B cells from cord blood	blood
36	chr11:65183800-65186400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr11:65183800-65187000	Flanking Active TSS	Thymus	Thymus
38	chr11:65183800-65187200	Flanking Active TSS	Primary B cells from peripheral blood	blood
39	chr11:65183800-65188600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr11:65183800-65188800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
41	chr11:65183800-65189600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
42	chr11:65183800-65189600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
43	chr11:65184000-65186400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr11:65184000-65187200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
45	chr11:65184000-65187200	Flanking Active TSS	NHDF-Ad	bronchial
46	chr11:65184000-65187800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr11:65184000-65187800	Flanking Active TSS	Fetal Thymus	thymus
48	chr11:65184000-65189200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr11:65184200-65187000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr11:65184200-65188800	Enhancers	HUES64 Cell Line	embryonic stem cell

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