Variant report

Variant	rs35267642
Chromosome Location	chr11:46391097-46391098
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	POLR2A	chr11:46390984-46391423	K562	blood:	n/a	n/a
2	RAD21	chr11:46390892-46391502	MCF-7	breast:	n/a	chr11:46391180-46391190 chr11:46391178-46391191 chr11:46391175-46391194
3	POLR2A	chr11:46391079-46391682	GM12878	blood:	n/a	n/a
4	RFX5	chr11:46391030-46391334	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr11:46391030-46391312	GM13977	blood:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
6	POLR2A	chr11:46390808-46391755	HL-60	blood:	n/a	n/a
7	CTCF	chr11:46391031-46391333	H1-hESC	embryonic stem cell:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
8	CTCF	chr11:46391002-46391312	ECC-1	luminal epithelium:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
9	CTCF	chr11:46390772-46391803	SK-N-SH	brain:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
10	RAD21	chr11:46391043-46391306	K562	blood:	n/a	chr11:46391180-46391190 chr11:46391178-46391191 chr11:46391175-46391194
11	CTCF	chr11:46390794-46391528	HCT-116	colon:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
12	CTCF	chr11:46391013-46391395	K562	blood:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
13	POLR2A	chr11:46390942-46391137	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr11:46391080-46391230	HL-60	blood:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391179-46391189
15	RCOR1	chr11:46391055-46391202	HepG2	liver:	n/a	n/a
16	CTCF	chr11:46391003-46391365	K562	blood:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
17	SMC3	chr11:46390883-46391954	SK-N-SH	brain:	n/a	chr11:46391176-46391183 chr11:46391284-46391298 chr11:46391284-46391294 chr11:46391287-46391295 chr11:46391176-46391190
18	CTCF	chr11:46390965-46391420	K562	blood:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
19	RAD21	chr11:46390903-46391441	A549	lung:	n/a	chr11:46391180-46391190 chr11:46391178-46391191 chr11:46391175-46391194
20	RAD21	chr11:46391000-46391363	Hela-S3	cervix:	n/a	chr11:46391180-46391190 chr11:46391178-46391191 chr11:46391175-46391194
21	CTCF	chr11:46391037-46391322	Hela-S3	cervix:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
22	CTCF	chr11:46390985-46391336	A549	lung:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
23	CTCF	chr11:46391080-46391230	AoAF	blood vessel:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391179-46391189
24	CTCF	chr11:46391026-46391354	T-47D	breast:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
25	CTCF	chr11:46391044-46391312	LNCaP	prostate:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
26	RCOR1	chr11:46390946-46391328	Hela-S3	cervix:	n/a	n/a
27	MAX	chr11:46390970-46391521	ECC-1	luminal epithelium:	n/a	n/a
28	RAD21	chr11:46391065-46391347	GM12878	blood:	n/a	chr11:46391180-46391190 chr11:46391178-46391191 chr11:46391175-46391194
29	MXI1	chr11:46390846-46391928	IMR90	lung:	n/a	n/a
30	WRNIP1	chr11:46391063-46391263	GM12878	blood:	n/a	n/a
31	JUN	chr11:46390992-46391199	H1-hESC	embryonic stem cell:	n/a	n/a
32	RCOR1	chr11:46391061-46391101	K562	blood:	n/a	n/a
33	RAD21	chr11:46390794-46391518	SK-N-SH	brain:	n/a	chr11:46391180-46391190 chr11:46391178-46391191 chr11:46391175-46391194
34	ZNF143	chr11:46390989-46391358	H1-hESC	embryonic stem cell:	n/a	n/a
35	SMC3	chr11:46390993-46391365	GM12878	blood:	n/a	chr11:46391176-46391183 chr11:46391284-46391298 chr11:46391284-46391294 chr11:46391287-46391295 chr11:46391176-46391190
36	CTCF	chr11:46390999-46391347	GM19240	blood:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
37	RAD21	chr11:46391041-46391390	H1-hESC	embryonic stem cell:	n/a	chr11:46391180-46391190 chr11:46391178-46391191 chr11:46391175-46391194
38	MAX	chr11:46390936-46391414	SK-N-SH	brain:	n/a	n/a
39	POLR2A	chr11:46390852-46391497	K562	blood:	n/a	n/a
40	EGR1	chr11:46391078-46391380	K562	blood:	n/a	n/a
41	CTCF	chr11:46391037-46391336	MCF-7	breast:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
42	CTCF	chr11:46391029-46391337	Fibrobl	skin:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
43	CTCF	chr11:46391040-46391298	HUVEC	blood vessel:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391284-46391297 chr11:46391179-46391189 chr11:46391285-46391295
44	CTCF	chr11:46391040-46391190	HVMF	connective:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391177-46391186 chr11:46391179-46391189
45	CTCF	chr11:46391020-46391170	HFF	foreskin:	n/a	n/a
46	RAD21	chr11:46391000-46391313	SK-N-SH_RA	brain:	n/a	chr11:46391180-46391190 chr11:46391178-46391191 chr11:46391175-46391194
47	BRCA1	chr11:46390991-46391191	Hela-S3	cervix:	n/a	n/a
48	MAX	chr11:46390934-46391469	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr11:46390931-46391352	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr11:46391080-46391230	GM12866	blood:	n/a	chr11:46391174-46391187 chr11:46391177-46391190 chr11:46391174-46391192 chr11:46391177-46391186 chr11:46391179-46391189

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46391053-46391103	SKMC	muscle:	n/a
2	chr11:46391053-46391103	MCF-7	breast:	n/a
3	chr11:46391053-46391103	HCPEpiC	choroid plexus:	n/a
4	chr11:46391053-46391103	ECC-1	luminal epithelium:	n/a
5	chr11:46391053-46391103	NT2-D1	testis:	n/a
6	chr11:46391053-46391103	PANC-1	pancreas:	n/a
7	chr11:46391053-46391103	HCF	heart:	n/a
8	chr11:46391053-46391103	HNPCEpiC	eye:	n/a
9	chr11:46391053-46391103	NH-A	brain:	n/a
10	chr11:46391053-46391103	ProgFib	skin:	n/a
11	chr11:46391053-46391103	HEEpiC	esophagus:	n/a
12	chr11:46391053-46391103	U87	brain:	n/a
13	chr11:46391053-46391103	Caco-2	colon:	n/a
14	chr11:46391053-46391103	HPAEpiC	pulmonary alveolar:	n/a
15	chr11:46391053-46391103	GM12878	blood:	n/a
16	chr11:46391053-46391103	SK-N-SH	brain:	n/a
17	chr11:46391053-46391103	HMEC	breast:	n/a
18	chr11:46391053-46391103	MCF10A-Er-Src	breast:	n/a
19	chr11:46391053-46391103	PFSK-1	brain:	n/a
20	chr11:46391053-46391103	H1-hESC	embryonic stem cell:	embryo
21	chr11:46391053-46391103	AG09319	gingival:	n/a
22	chr11:46391053-46391103	GM12892	blood:	n/a
23	chr11:46391053-46391103	HUVEC	blood vessel:	n/a
24	chr11:46391053-46391103	HRPEpiC	eye:	n/a
25	chr11:46391053-46391103	GM19239	blood:	n/a
26	chr11:46391053-46391103	NHBE	bronchial:	n/a
27	chr11:46391053-46391103	AoSMC	blood vessel:	n/a
28	chr11:46391053-46391103	CMK	blood:	n/a
29	chr11:46391053-46391103	BE2_C	brain:	n/a
30	chr11:46391053-46391103	GM06990	blood:	n/a
31	chr11:46391053-46391103	HCM	heart:	n/a
32	chr11:46391053-46391103	A549	lung:	n/a
33	chr11:46391053-46391103	ovcar-3	ovarian:	n/a
34	chr11:46391053-46391103	GM12891	blood:	n/a
35	chr11:46391053-46391103	SK-N-SH_RA	brain:	n/a
36	chr11:46391053-46391103	LNCaP	prostate:	n/a
37	chr11:46391053-46391103	HL-60	blood:	n/a
38	chr11:46391053-46391103	HRE	kidney:	n/a
39	chr11:46391053-46391103	HepG2	liver:	n/a
40	chr11:46391053-46391103	SK-N-MC	brain:	n/a
41	chr11:46391053-46391103	NB4	blood:	n/a
42	chr11:46391053-46391103	K562	blood:	n/a
43	chr11:46391053-46391103	Jurkat	blood:	n/a
44	chr11:46391053-46391103	AG09309	skin:	n/a
45	chr11:46391053-46391103	PrEC	prostate:	n/a
46	chr11:46391053-46391103	Hepatocyte	liver:	n/a
47	chr11:46391053-46391103	RPTEC	kidney:	n/a
48	chr11:46391053-46391103	HRCEpiC	kidney:	n/a
49	chr11:46391053-46391103	BJ	skin:	n/a
50	chr11:46391053-46391103	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:46261225..46262867-chr11:46390167..46391746,2	K562	blood:
2	chr11:46336682..46337395-chr11:46390775..46391616,2	MCF-7	breast:
3	chr11:46390753..46391347-chr8:145539335..145539909,2	MCF-7	breast:
4	chr11:46259184..46261367-chr11:46390797..46392907,2	MCF-7	breast:
5	chr11:46390741..46391631-chr11:46413418..46414279,3	MCF-7	breast:
6	chr11:46390154..46392159-chr11:46397767..46399313,2	MCF-7	breast:
7	chr11:46390882..46391665-chr11:46559110..46559652,3	K562	blood:
8	chr11:46390694..46391646-chr11:46559109..46559709,2	MCF-7	breast:
9	chr11:46373344..46374865-chr11:46390768..46391595,4	MCF-7	breast:

Variant related genes	Relation type
DGKZ	TF binding region
DGKZ	CpG island
ENSG00000157613	Chromatin interaction
ENSG00000149091	Chromatin interaction
ENSG00000264102	Chromatin interaction
ENSG00000254639	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10734546	1.00[AMR][1000 genomes]
rs1489190	1.00[AMR][1000 genomes]
rs1812657	1.00[AMR][1000 genomes]
rs1873129	1.00[AMR][1000 genomes]
rs2029378	1.00[AMR][1000 genomes]
rs2046766	1.00[AMR][1000 genomes]
rs2046767	1.00[AMR][1000 genomes]
rs2087360	1.00[AMR][1000 genomes]
rs2087361	1.00[AMR][1000 genomes]
rs2864071	1.00[AMR][1000 genomes]
rs34217002	1.00[AMR][1000 genomes]
rs34444424	1.00[AMR][1000 genomes]
rs35715394	1.00[AMR][1000 genomes]
rs35935319	1.00[AMR][1000 genomes]
rs4367921	1.00[AMR][1000 genomes]
rs4376875	1.00[AMR][1000 genomes]
rs4433539	1.00[AMR][1000 genomes]
rs4508179	1.00[AMR][1000 genomes]
rs4550197	1.00[AMR][1000 genomes]
rs56991558	1.00[AMR][1000 genomes]
rs58314136	1.00[AMR][1000 genomes]
rs58770070	1.00[AMR][1000 genomes]
rs60162610	1.00[AMR][1000 genomes]
rs61451984	1.00[AMR][1000 genomes]
rs61514976	1.00[AMR][1000 genomes]
rs61693609	1.00[AMR][1000 genomes]
rs6485681	1.00[AMR][1000 genomes]
rs73464080	1.00[AMR][1000 genomes]
rs73466031	1.00[AMR][1000 genomes]
rs73466069	1.00[AMR][1000 genomes]
rs73466088	1.00[AMR][1000 genomes]
rs73466094	1.00[AMR][1000 genomes]
rs73466095	1.00[AMR][1000 genomes]
rs73466099	1.00[AMR][1000 genomes]
rs73467917	1.00[AMR][1000 genomes]
rs73467919	1.00[AMR][1000 genomes]
rs73467920	1.00[AMR][1000 genomes]
rs73467936	1.00[AMR][1000 genomes]
rs73467938	1.00[AMR][1000 genomes]
rs73467941	1.00[AMR][1000 genomes]
rs73467944	1.00[AMR][1000 genomes]
rs73467950	1.00[AMR][1000 genomes]
rs73467963	1.00[AMR][1000 genomes]
rs7924695	1.00[AMR][1000 genomes]
rs7928869	1.00[AMR][1000 genomes]
rs967754	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv554201	chr11:46281835-46422686	Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv825867	chr11:46303184-46425613	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS 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	21 gene(s)	inside rSNPs	diseases
3	esv1797501	chr11:46315437-46402521	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
4	esv1811345	chr11:46317062-46438072	Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers 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	22 gene(s)	inside rSNPs	diseases
5	nsv554202	chr11:46334239-46469900	Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers 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	25 gene(s)	inside rSNPs	diseases
6	nsv897316	chr11:46349631-46417815	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
7	nsv897317	chr11:46363411-46417815	Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
8	nsv897318	chr11:46388220-46417815	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46370000-46395800	Weak transcription	Aorta	Aorta
2	chr11:46383600-46392200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:46383600-46402000	Weak transcription	Fetal Brain Male	brain
4	chr11:46384200-46391800	Genic enhancers	Primary T cells fromperipheralblood	blood
5	chr11:46384400-46391600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr11:46384800-46395600	Weak transcription	Small Intestine	intestine
7	chr11:46385200-46391600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr11:46385200-46393000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr11:46385200-46400600	Strong transcription	Thymus	Thymus
10	chr11:46385400-46401200	Strong transcription	Dnd41	blood
11	chr11:46385600-46391200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:46386000-46398200	Weak transcription	Primary B cells from cord blood	blood
13	chr11:46386000-46402200	Weak transcription	NHDF-Ad	bronchial
14	chr11:46386200-46392000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr11:46386400-46395400	Weak transcription	Psoas Muscle	Psoas
16	chr11:46386600-46396000	Genic enhancers	Fetal Muscle Trunk	muscle
17	chr11:46387200-46399200	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr11:46387600-46396800	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr11:46388000-46392200	Strong transcription	GM12878-XiMat	blood
20	chr11:46388400-46393200	Strong transcription	Duodenum Mucosa	Duodenum
21	chr11:46388600-46391800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr11:46388600-46396200	Genic enhancers	Fetal Muscle Leg	muscle
23	chr11:46388600-46400200	Strong transcription	Gastric	stomach
24	chr11:46388800-46400600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr11:46389000-46391200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr11:46389000-46391200	Strong transcription	Lung	lung
27	chr11:46389000-46391600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr11:46389000-46399600	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr11:46389000-46399600	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr11:46389000-46402000	Weak transcription	Right Atrium	heart
31	chr11:46389400-46391600	Genic enhancers	A549	lung
32	chr11:46389400-46400200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
33	chr11:46389400-46400400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr11:46389400-46401400	Strong transcription	Primary T cells from cord blood	blood
35	chr11:46389600-46391200	Strong transcription	H1 Cell Line	embryonic stem cell
36	chr11:46389600-46391200	Strong transcription	Fetal Intestine Small	intestine
37	chr11:46389600-46391600	Weak transcription	Primary B cells from peripheral blood	blood
38	chr11:46389600-46391600	Weak transcription	Colonic Mucosa	Colon
39	chr11:46389600-46391600	Genic enhancers	HMEC	breast
40	chr11:46389600-46392000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr11:46389600-46392000	Strong transcription	Rectal Smooth Muscle	rectum
42	chr11:46389600-46392400	Strong transcription	NHEK	skin
43	chr11:46389600-46393800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr11:46389600-46394400	Strong transcription	Esophagus	oesophagus
45	chr11:46389600-46394600	Strong transcription	Primary hematopoietic stem cells	blood
46	chr11:46389600-46396600	Weak transcription	Fetal Lung	lung
47	chr11:46389600-46397000	Strong transcription	Spleen	Spleen
48	chr11:46389600-46398400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
49	chr11:46389600-46399200	Strong transcription	Right Ventricle	heart
50	chr11:46389600-46399800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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