Variant report

Variant	rs3802941
Chromosome Location	chr11:63682869-63682870
allele	C/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	RAD21	chr11:63682620-63684442	SK-N-SH	brain:	n/a	chr11:63682798-63682808 chr11:63684308-63684321 chr11:63684016-63684035 chr11:63682798-63682810 chr11:63683940-63683953 chr11:63682796-63682809 chr11:63683756-63683766
2	CTCF	chr11:63682720-63682870	HCM	heart:	n/a	n/a
3	POLR2A	chr11:63682813-63682919	K562	blood:	n/a	n/a
4	POLR2A	chr11:63682527-63682931	H1-hESC	embryonic stem cell:	n/a	n/a
5	RAD21	chr11:63682659-63682912	SK-N-SH_RA	brain:	n/a	chr11:63682798-63682808 chr11:63682798-63682810 chr11:63682796-63682809
6	RAD21	chr11:63682718-63682880	SK-N-SH_RA	brain:	n/a	chr11:63682798-63682808 chr11:63682798-63682810 chr11:63682796-63682809
7	POLR2A	chr11:63681342-63683085	H1-hESC	embryonic stem cell:	n/a	n/a
8	MXI1	chr11:63682495-63686664	SK-N-SH	brain:	n/a	chr11:63684285-63684294
9	SMC3	chr11:63682501-63684951	SK-N-SH	brain:	n/a	chr11:63682772-63682779 chr11:63682956-63682966 chr11:63683582-63683592 chr11:63684771-63684785
10	CTCF	chr11:63682744-63682871	GM12892	blood:	n/a	n/a
11	CTCF	chr11:63682800-63682950	NB4	blood:	n/a	n/a
12	POLR2A	chr11:63682810-63683033	ProgFib	skin:	n/a	n/a
13	CTCF	chr11:63682737-63682890	MCF-7	breast:	n/a	n/a
14	CTCF	chr11:63682740-63682890	WERI-Rb-1	eye:	n/a	n/a
15	POLR2A	chr11:63682587-63682873	HCT-116	colon:	n/a	n/a
16	MAZ	chr11:63682812-63682878	K562	blood:	n/a	n/a
17	RAD21	chr11:63682543-63682995	H1-hESC	embryonic stem cell:	n/a	chr11:63682798-63682808 chr11:63682798-63682810 chr11:63682796-63682809
18	CTCF	chr11:63682720-63682870	SK-N-SH_RA	brain:	n/a	n/a
19	POLR2A	chr11:63682354-63682971	SK-N-MC	brain:	n/a	n/a
20	CTCF	chr11:63682720-63682870	HepG2	liver:	n/a	n/a
21	CTCF	chr11:63682760-63682910	HMEC	breast:	n/a	n/a
22	POLR2A	chr11:63682114-63682917	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:63674570..63680304-chr11:63681753..63686803,9	MCF-7	breast:
2	chr11:63682847..63685544-chr11:63752668..63755278,2	MCF-7	breast:
3	chr11:63668978..63670903-chr11:63681727..63683409,2	K562	blood:
4	chr11:63680773..63683406-chr11:63684086..63687112,3	MCF-7	breast:
5	chr11:63682437..63684177-chr8:101963345..101965664,2	MCF-7	breast:
6	chr11:63682343..63688338-chr11:63931257..63935493,5	K562	blood:
7	chr11:63666544..63671236-chr11:63682476..63685803,4	MCF-7	breast:
8	chr11:63673944..63681438-chr11:63681488..63685981,13	K562	blood:
9	chr11:63579193..63582428-chr11:63682051..63685961,4	K562	blood:
10	chr11:63682242..63690244-chr11:63703955..63713214,18	K562	blood:
11	chr11:63580176..63582428-chr11:63682563..63684680,2	K562	blood:

Variant related genes	Relation type
RCOR2	TF binding region
ENSG00000072518	Chromatin interaction
ENSG00000167770	Chromatin interaction
ENSG00000168005	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000110583	Chromatin interaction
ENSG00000167771	Chromatin interaction
ENSG00000164924	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10736731	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];1.00[LWK][hapmap];0.94[MEX][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10751001	0.85[ASN][1000 genomes]
rs10792421	0.92[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.88[LWK][hapmap];0.89[MEX][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10792422	1.00[CHB][hapmap];0.87[YRI][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10792423	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10897452	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10897453	0.87[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.88[LWK][hapmap];0.87[MKK][hapmap];0.86[YRI][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10897454	0.87[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.88[LWK][hapmap];0.87[MKK][hapmap];0.88[YRI][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11231600	0.92[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.81[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11231624	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11231628	0.86[CHB][hapmap];0.81[JPT][hapmap];0.90[ASN][1000 genomes]
rs11231637	0.92[CEU][hapmap];0.91[GIH][hapmap];0.94[MEX][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11231640	0.80[ASW][hapmap];0.88[CEU][hapmap];0.93[CHB][hapmap];0.89[GIH][hapmap];0.81[JPT][hapmap];0.81[LWK][hapmap];0.89[MEX][hapmap];0.81[YRI][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11605500	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12277481	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12576275	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1486936	0.92[CEU][hapmap];0.91[GIH][hapmap];0.94[MEX][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1872772	0.94[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.93[LWK][hapmap];0.94[MEX][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2318110	0.83[ASN][1000 genomes]
rs2840079	0.88[CEU][hapmap];0.82[CHB][hapmap];0.86[GIH][hapmap];0.89[MEX][hapmap];0.81[YRI][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs320109	0.92[CEU][hapmap];0.91[GIH][hapmap];0.89[MEX][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3850943	0.85[ASN][1000 genomes]
rs4143327	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4963433	0.85[ASN][1000 genomes]
rs4980503	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4980505	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4980507	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4980528	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];1.00[LWK][hapmap];0.94[MEX][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4980529	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.94[MEX][hapmap];0.94[YRI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4980532	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4980533	0.94[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];1.00[LWK][hapmap];0.94[MEX][hapmap];0.96[MKK][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]
rs6421686	0.87[EUR][1000 genomes]
rs6591825	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.96[LWK][hapmap];0.94[MEX][hapmap];0.89[MKK][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7102006	0.92[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.83[YRI][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7105288	0.92[CEU][hapmap];0.91[GIH][hapmap];0.94[MEX][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7108375	0.92[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7110843	0.94[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.96[LWK][hapmap];0.94[MEX][hapmap];0.89[MKK][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7118913	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];1.00[LWK][hapmap];0.94[MEX][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7121067	0.94[EUR][1000 genomes]
rs7937314	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7939416	0.80[ASN][1000 genomes]
rs7944519	0.87[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.88[LWK][hapmap];0.89[MEX][hapmap];0.87[MKK][hapmap];0.88[YRI][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7948656	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs923247	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs928948	0.86[CHB][hapmap];0.81[JPT][hapmap];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer 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	100 gene(s)	inside rSNPs	diseases
2	nsv468589	chr11:63515752-63713239	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv555180	chr11:63515752-63713239	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS 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 target site	39 gene(s)	inside rSNPs	diseases
4	nsv468590	chr11:63639881-63783352	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv555181	chr11:63639881-63783352	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv897629	chr11:63664882-63866959	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
7	nsv897630	chr11:63664882-63924446	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh 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	46 gene(s)	inside rSNPs	diseases
8	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
9	nsv897632	chr11:63670787-63688693	Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
10	nsv897633	chr11:63670787-63691049	Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv897634	chr11:63670787-63698538	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
12	nsv897635	chr11:63674926-63688693	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv897636	chr11:63676067-63688693	Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
14	nsv897637	chr11:63676067-63691049	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
15	nsv897638	chr11:63676562-63688693	Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63669600-63683200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr11:63670000-63683200	Weak transcription	K562	blood
3	chr11:63670000-63683400	Weak transcription	HSMM	muscle
4	chr11:63671000-63683800	Weak transcription	NHDF-Ad	bronchial
5	chr11:63672400-63683200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr11:63672400-63683800	Weak transcription	Psoas Muscle	Psoas
7	chr11:63673200-63683200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr11:63676200-63683400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr11:63676400-63683400	Weak transcription	Brain Substantia Nigra	brain
10	chr11:63676400-63683400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr11:63676600-63683400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:63676600-63683400	Weak transcription	Brain Angular Gyrus	brain
13	chr11:63676600-63684000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:63676600-63684000	Weak transcription	Aorta	Aorta
15	chr11:63676800-63683200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr11:63676800-63683200	Weak transcription	Duodenum Mucosa	Duodenum
17	chr11:63676800-63683200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr11:63676800-63683400	Weak transcription	HMEC	breast
19	chr11:63677000-63683400	Weak transcription	Hela-S3	cervix
20	chr11:63677000-63683600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr11:63677600-63683400	Weak transcription	Ovary	ovary
22	chr11:63677800-63683200	Weak transcription	Dnd41	blood
23	chr11:63677800-63683400	Weak transcription	Colon Smooth Muscle	Colon
24	chr11:63677800-63683400	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr11:63678000-63683200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr11:63678000-63683200	Weak transcription	Thymus	Thymus
27	chr11:63678000-63683200	Weak transcription	NHLF	lung
28	chr11:63678000-63683400	Weak transcription	Liver	Liver
29	chr11:63678400-63683200	Weak transcription	Primary B cells from cord blood	blood
30	chr11:63678400-63683400	Weak transcription	Pancreas	Pancrea
31	chr11:63678400-63683600	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr11:63678600-63683200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr11:63678600-63683400	Weak transcription	A549	lung
34	chr11:63678800-63683600	Weak transcription	Primary hematopoietic stem cells	blood
35	chr11:63679200-63683200	Weak transcription	Small Intestine	intestine
36	chr11:63679200-63683400	Weak transcription	Primary T cells from cord blood	blood
37	chr11:63679200-63684000	Weak transcription	HSMMtube	muscle
38	chr11:63680400-63683200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr11:63680600-63683400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr11:63681400-63683000	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:63681800-63683000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:63681800-63683400	Enhancers	Fetal Brain Male	brain
43	chr11:63682200-63683200	Enhancers	Fetal Lung	lung
44	chr11:63682400-63683000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr11:63682400-63683000	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
46	chr11:63682400-63683200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr11:63682400-63683200	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr11:63682400-63683400	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr11:63682400-63683400	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr11:63682400-63683400	Enhancers	Fetal Heart	heart

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