Variant report

Variant	rs641018
Chromosome Location	chr11:65655393-65655394
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	CTCF	chr11:65654850-65657446	SK-N-SH	brain:	n/a	chr11:65656106-65656119
2	RAD21	chr11:65655359-65656794	IMR90	lung:	n/a	chr11:65656248-65656260 chr11:65655946-65655960
3	CTCF	chr11:65655360-65655510	SAEC	small airway:	n/a	n/a
4	MAX	chr11:65655268-65656890	A549	lung:	n/a	chr11:65655739-65655749
5	POLR2A	chr11:65654926-65656797	SK-N-MC	brain:	n/a	n/a
6	SPI1	chr11:65655375-65656499	HL-60	blood:	n/a	n/a
7	POLR2A	chr11:65654632-65669034	U87	brain:	n/a	n/a
8	ZNF263	chr11:65655304-65656286	K562	blood:	n/a	n/a
9	POLR2A	chr11:65655284-65657061	ProgFib	skin:	n/a	n/a
10	ELF1	chr11:65655369-65656862	SK-N-SH	brain:	n/a	chr11:65655962-65655971 chr11:65656015-65656024 chr11:65655961-65655972 chr11:65656014-65656025 chr11:65655961-65655972
11	HA-E2F1	chr11:65655338-65656299	MCF-7	breast:	n/a	chr11:65656046-65656058 chr11:65655944-65655953 chr11:65655765-65655774 chr11:65655738-65655747
12	E2F6	chr11:65655295-65656586	A549	lung:	n/a	chr11:65656046-65656058 chr11:65655944-65655953 chr11:65655765-65655774 chr11:65655738-65655747 chr11:65656047-65656058 chr11:65656058-65656069
13	NFIC	chr11:65655336-65656335	GM12878	blood:	n/a	chr11:65655929-65655957
14	POLR2A	chr11:65655369-65656337	Hela-S3	cervix:	n/a	n/a
15	MAX	chr11:65655267-65656592	H1-hESC	embryonic stem cell:	n/a	chr11:65655739-65655749
16	MYC	chr11:65655362-65655585	MCF-7	breast:	n/a	n/a
17	RUNX3	chr11:65655262-65656894	GM12878	blood:	n/a	n/a
18	MAX	chr11:65655189-65656699	K562	blood:	n/a	chr11:65655739-65655749
19	CTCF	chr11:65655320-65655470	HRPEpiC	eye:	n/a	n/a
20	SIN3A	chr11:65655370-65656766	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr11:65655144-65662194	HUVEC	blood vessel:	n/a	n/a
22	POLR2A	chr11:65655269-65656390	HL-60	blood:	n/a	n/a
23	POLR2A	chr11:65655375-65656933	HUVEC	blood vessel:	n/a	n/a
24	GABPA	chr11:65655266-65656654	MCF-7	breast:	n/a	chr11:65655738-65655747 chr11:65656387-65656398
25	CTCF	chr11:65655357-65656271	K562	blood:	n/a	chr11:65656106-65656119
26	MYC	chr11:65655309-65656204	MCF-7	breast:	n/a	chr11:65655739-65655749
27	CTCF	chr11:65655322-65656821	HCT-116	colon:	n/a	chr11:65656106-65656119
28	TAF1	chr11:65655359-65656361	H1-neurons	neurons:	n/a	n/a
29	SIN3AK20	chr11:65655313-65656436	MCF-7	breast:	n/a	n/a
30	MAX	chr11:65655324-65656405	Hela-S3	cervix:	n/a	chr11:65655739-65655749
31	TAF1	chr11:65655361-65656428	H1-neurons	neurons:	n/a	n/a
32	E2F6	chr11:65655342-65655632	K562	blood:	n/a	n/a
33	MYC	chr11:65655354-65656616	K562	blood:	n/a	chr11:65655739-65655749
34	SMC3	chr11:65655371-65656320	Hela-S3	cervix:	n/a	n/a
35	RCOR1	chr11:65655259-65656304	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr11:65655336-65656367	A549	lung:	n/a	n/a
37	POLR2A	chr11:65655268-65656650	H1-neurons	neurons:	n/a	n/a
38	TAF1	chr11:65655255-65656562	ECC-1	luminal epithelium:	n/a	n/a
39	CBX3	chr11:65655249-65656766	K562	blood:	n/a	n/a
40	GABPA	chr11:65655378-65656749	SK-N-SH	brain:	n/a	chr11:65655738-65655747 chr11:65656387-65656398
41	CREB1	chr11:65655300-65656329	H1-hESC	embryonic stem cell:	n/a	n/a
42	ZNF263	chr11:65655314-65656763	HEK293-T-REx	kidney:	n/a	n/a
43	YY1	chr11:65655316-65656329	K562	blood:	n/a	chr11:65655738-65655747
44	GABPA	chr11:65655298-65656680	A549	lung:	n/a	chr11:65655738-65655747 chr11:65656387-65656398
45	POLR2A	chr11:65655319-65657029	K562	blood:	n/a	n/a
46	SIN3AK20	chr11:65655316-65656889	SK-N-SH	brain:	n/a	n/a
47	MAX	chr11:65655240-65656746	ECC-1	luminal epithelium:	n/a	chr11:65655739-65655749
48	MAZ	chr11:65654781-65660027	IMR90	lung:	n/a	chr11:65658152-65658161 chr11:65658196-65658205 chr11:65655739-65655749
49	JUN	chr11:65655320-65656833	K562	blood:	n/a	chr11:65655630-65655639 chr11:65656398-65656412
50	GABPA	chr11:65655319-65656493	SK-N-SH	brain:	n/a	chr11:65655738-65655747 chr11:65656387-65656398

No.	Distal block	Cell Line	Cell type
1	chr11:65651325..65654107-chr11:65654178..65656416,6	MCF-7	breast:
2	chr11:65654814..65656550-chr11:65837621..65839885,2	MCF-7	breast:
3	chr11:65650800..65661192-chr11:65726307..65736419,31	MCF-7	breast:
4	chr11:65652640..65657924-chr11:65769844..65772901,4	MCF-7	breast:
5	chr11:65428955..65432251-chr11:65654758..65658672,5	K562	blood:
6	chr11:65381281..65383865-chr11:65653428..65656647,3	MCF-7	breast:
7	chr11:65551697..65554555-chr11:65655334..65658299,2	K562	blood:
8	chr11:65654573..65660022-chr11:65726606..65732418,16	MCF-7	breast:
9	chr11:65653872..65655439-chr11:65819270..65821819,2	K562	blood:
10	chr11:65650579..65663306-chr11:65677153..65690311,39	MCF-7	breast:
11	chr11:65654594..65656480-chr11:65848880..65851795,2	K562	blood:
12	chr11:65478611..65480184-chr11:65654546..65656636,2	MCF-7	breast:
13	chr11:65343312..65345815-chr11:65654213..65655812,2	MCF-7	breast:
14	chr11:65654924..65661575-chr11:65833688..65838665,10	K562	blood:
15	chr11:65478350..65482284-chr11:65653854..65660529,8	K562	blood:
16	chr11:65557488..65562536-chr11:65655379..65657877,5	K562	blood:
17	chr11:65654924..65660442-chr11:65834310..65838665,6	K562	blood:
18	chr11:65429800..65432139-chr11:65653071..65655699,2	MCF-7	breast:
19	chr11:65485673..65489789-chr11:65654054..65658887,6	K562	blood:
20	chr11:65477188..65481209-chr11:65654091..65661409,11	K562	blood:
21	chr11:65557488..65560218-chr11:65655379..65657652,3	K562	blood:
22	chr11:65478149..65481961-chr11:65654535..65657747,6	MCF-7	breast:
23	chr11:65654406..65656554-chr11:65818022..65819720,2	MCF-7	breast:
24	chr11:65646632..65650808-chr11:65654844..65660529,6	MCF-7	breast:

Variant related genes	Relation type
FIBP	TF binding region
CCDC85B	TF binding region
ENSG00000172818	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000175573	Chromatin interaction
ENSG00000172543	Chromatin interaction
ENSG00000175550	Chromatin interaction
ENSG00000172977	Chromatin interaction
ENSG00000173039	Chromatin interaction
ENSG00000172922	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000172500	Chromatin interaction
ENSG00000255038	Chromatin interaction
ENSG00000087365	Chromatin interaction
ENSG00000255120	Chromatin interaction
ENSG00000175467	Chromatin interaction
ENSG00000173442	Chromatin interaction
ENSG00000175115	Chromatin interaction
ENSG00000175334	Chromatin interaction
ENSG00000238752	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 21 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10791830	0.88[CEU][hapmap];0.95[CHB][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1151519	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1204650	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12225345	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2231884	0.81[JPT][hapmap];0.86[EUR][1000 genomes]
rs2303385	0.83[CHB][hapmap];0.86[YRI][hapmap]
rs507062	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs568617	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs583887	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs585557	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs58568715	0.84[EUR][1000 genomes]
rs588114	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs596002	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs601863	0.83[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs608616	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs622614	0.88[CEU][hapmap];0.95[CHB][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs625652	0.85[AFR][1000 genomes]
rs645900	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs656980	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs658524	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs658938	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs677931	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs687672	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs693824	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs694994	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7940691	0.83[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897736	chr11:65335705-65676516	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' 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	227 gene(s)	inside rSNPs	diseases
2	nsv430401	chr11:65419324-65788024	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
3	esv2758274	chr11:65559893-65722363	Genic enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
4	esv2759834	chr11:65559893-65722363	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
5	nsv427890	chr11:65559893-65722363	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
6	nsv897761	chr11:65580638-65738566	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	186 gene(s)	inside rSNPs	diseases
7	nsv555215	chr11:65581579-65676516	Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers 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	165 gene(s)	inside rSNPs	diseases
8	nsv897762	chr11:65613218-65758854	Active TSS Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	185 gene(s)	inside rSNPs	diseases
9	nsv897764	chr11:65613348-65695222	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
10	nsv897765	chr11:65623708-65758854	Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
11	nsv832191	chr11:65632329-65806120	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
12	nsv530622	chr11:65649068-65661361	Genic enhancers Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	65 gene(s)	inside rSNPs	diseases

mRNA abundance (count:21)

SNP	Gene	Cis/trans	Tissue	Source
rs641018	SNX32	cis	Artery Tibial	GTEx
rs641018	SNX32	cis	Artery Aorta	GTEx
rs641018	CTSW	cis	Artery Aorta	GTEx
rs641018	CTSW	cis	Thyroid	GTEx
rs641018	CTSW	cis	Esophagus Mucosa	GTEx
rs641018	SNX32	cis	Esophagus Muscularis	GTEx
rs641018	SNX32	cis	Nerve Tibial	GTEx
rs641018	CTSW	cis	Whole Blood	GTEx
rs641018	FIBP	Cis_1M	lymphoblastoid	RTeQTL
rs641018	CTSW	cis	Lymphoblastoid	GTEx
rs641018	CTSW	cis	Stomach	GTEx
rs641018	CTSW	cis	Artery Tibial	GTEx
rs641018	CTSW	cis	Esophagus Muscularis	GTEx
rs641018	SNX32	cis	Esophagus Mucosa	GTEx
rs641018	CTSW	Cis_1M	lymphoblastoid	RTeQTL
rs641018	FIBP	cis	multi-tissue	Pritchard
rs641018	CTSW	cis	multi-tissue	Pritchard
rs641018	FIBP	cis	Lymphoblastoid	GTEx
rs641018	CTSW	cis	Nerve Tibial	GTEx
rs641018	SNX32	cis	Thyroid	GTEx
rs641018	CTSW	cis	lung	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65654000-65655400	Weak transcription	Ovary	ovary
2	chr11:65654000-65655400	Enhancers	Small Intestine	intestine
3	chr11:65654400-65655400	Flanking Active TSS	Fetal Brain Female	brain
4	chr11:65654600-65655400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
5	chr11:65654600-65655400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr11:65654600-65655400	Flanking Active TSS	Hela-S3	cervix
7	chr11:65654600-65655600	Flanking Active TSS	Brain Germinal Matrix	brain
8	chr11:65654600-65656400	Active TSS	A549	lung
9	chr11:65654600-65657200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:65654800-65655400	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr11:65654800-65655400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
12	chr11:65654800-65655400	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr11:65654800-65655400	Flanking Active TSS	NHDF-Ad	bronchial
14	chr11:65654800-65655600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:65654800-65655600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:65654800-65655600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
17	chr11:65654800-65655600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
18	chr11:65654800-65655800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
19	chr11:65654800-65655800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr11:65654800-65656000	Flanking Active TSS	HMEC	breast
21	chr11:65654800-65656600	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr11:65655000-65655400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr11:65655000-65655400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr11:65655000-65655400	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr11:65655000-65655400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr11:65655000-65655400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr11:65655000-65655400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr11:65655000-65655400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr11:65655000-65655400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr11:65655000-65655400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr11:65655000-65655400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr11:65655000-65655400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr11:65655000-65655400	Flanking Active TSS	Brain Anterior Caudate	brain
34	chr11:65655000-65655400	Flanking Active TSS	Fetal Brain Male	brain
35	chr11:65655000-65655400	Flanking Active TSS	Fetal Heart	heart
36	chr11:65655000-65655400	Flanking Active TSS	Fetal Kidney	kidney
37	chr11:65655000-65655400	Flanking Active TSS	Left Ventricle	heart
38	chr11:65655000-65655400	Enhancers	Spleen	Spleen
39	chr11:65655000-65655400	Flanking Active TSS	GM12878-XiMat	blood
40	chr11:65655000-65655400	Flanking Active TSS	HepG2	liver
41	chr11:65655000-65655400	Flanking Active TSS	HSMMtube	muscle
42	chr11:65655000-65655400	Flanking Active TSS	K562	blood
43	chr11:65655000-65655400	Flanking Active TSS	NH-A	brain
44	chr11:65655000-65655400	Flanking Active TSS	NHLF	lung
45	chr11:65655000-65655600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr11:65655000-65655600	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:65655000-65655600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
48	chr11:65655000-65655600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr11:65655000-65655600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
50	chr11:65655000-65655600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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