Variant report

Variant	rs7638204
Chromosome Location	chr3:52278241-52278242
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	RCOR1	chr3:52278092-52279638	GM12878	blood:	n/a	n/a
2	FOS	chr3:52278076-52278661	MCF10A-Er-Src	breast:	n/a	chr3:52278232-52278240 chr3:52278231-52278241 chr3:52278504-52278514 chr3:52278233-52278240 chr3:52278231-52278241 chr3:52278232-52278240 chr3:52278503-52278515 chr3:52278231-52278241 chr3:52278504-52278514 chr3:52278231-52278241
3	POLR2A	chr3:52278018-52278642	GM18526	blood:	n/a	n/a
4	POLR2A	chr3:52278000-52278774	GM12878	blood:	n/a	n/a
5	BATF	chr3:52278012-52278689	GM12878	blood:	n/a	chr3:52278229-52278239
6	STAT3	chr3:52278173-52278598	MCF10A-Er-Src	breast:	n/a	chr3:52278528-52278535
7	POLR2A	chr3:52277914-52278672	U87	brain:	n/a	n/a
8	EBF1	chr3:52277964-52278644	GM12878	blood:	n/a	n/a
9	POLR2A	chr3:52278063-52279526	GM12878	blood:	n/a	n/a
10	POU2F2	chr3:52278034-52278673	GM12891	blood:	n/a	n/a
11	FOS	chr3:52278076-52278644	MCF10A-Er-Src	breast:	n/a	chr3:52278232-52278240 chr3:52278231-52278241 chr3:52278504-52278514 chr3:52278233-52278240 chr3:52278231-52278241 chr3:52278232-52278240 chr3:52278503-52278515 chr3:52278231-52278241 chr3:52278504-52278514 chr3:52278231-52278241
12	POLR2A	chr3:52278009-52278506	U87	brain:	n/a	n/a
13	ZNF143	chr3:52278066-52278634	GM12878	blood:	n/a	n/a
14	POLR2A	chr3:52277359-52278451	K562	blood:	n/a	n/a
15	MTA3	chr3:52277652-52279590	GM12878	blood:	n/a	n/a
16	FOS	chr3:52278076-52278663	MCF10A-Er-Src	breast:	n/a	chr3:52278232-52278240 chr3:52278231-52278241 chr3:52278504-52278514 chr3:52278233-52278240 chr3:52278231-52278241 chr3:52278232-52278240 chr3:52278503-52278515 chr3:52278231-52278241 chr3:52278504-52278514 chr3:52278231-52278241
17	MYC	chr3:52278182-52278623	MCF10A-Er-Src	breast:	n/a	chr3:52278231-52278240
18	TBL1XR1	chr3:52278076-52279621	GM12878	blood:	n/a	n/a
19	RUNX3	chr3:52277852-52279708	GM12878	blood:	n/a	n/a
20	YY1	chr3:52277973-52278342	GM12878	blood:	n/a	n/a
21	STAT5A	chr3:52277938-52278700	GM12878	blood:	n/a	chr3:52278528-52278535 chr3:52277940-52277952
22	POLR2A	chr3:52277921-52279621	GM12892	blood:	n/a	n/a
23	POLR2A	chr3:52277912-52278629	HCT-116	colon:	n/a	n/a
24	MXI1	chr3:52278104-52278584	GM12878	blood:	n/a	n/a
25	IKZF1	chr3:52278160-52279282	GM12878	blood:	n/a	n/a
26	POLR2A	chr3:52277954-52280665	GM12878	blood:	n/a	n/a
27	POLR2A	chr3:52278140-52278582	Hela-S3	cervix:	n/a	n/a
28	EBF1	chr3:52278051-52278635	GM12878	blood:	n/a	n/a
29	MYC	chr3:52278045-52278631	MCF10A-Er-Src	breast:	n/a	chr3:52278231-52278240
30	SPI1	chr3:52278096-52278766	GM12891	blood:	n/a	chr3:52278471-52278484
31	MAX	chr3:52278125-52278586	GM12878	blood:	n/a	chr3:52278231-52278240
32	RELA	chr3:52277935-52278646	GM15510	blood:	n/a	n/a
33	FOXM1	chr3:52278021-52279327	GM12878	blood:	n/a	n/a
34	ZEB1	chr3:52277881-52278670	GM12878	blood:	n/a	n/a
35	POLR2A	chr3:52277713-52280381	GM18505	blood:	n/a	n/a
36	EGR1	chr3:52277809-52278697	HCT-116	colon:	n/a	chr3:52277943-52277952 chr3:52278243-52278258
37	EGR1	chr3:52278118-52278626	GM12878	blood:	n/a	chr3:52278243-52278258
38	NFIC	chr3:52277976-52279304	GM12878	blood:	n/a	n/a
39	ATF2	chr3:52278011-52279283	GM12878	blood:	n/a	n/a
40	GTF2F1	chr3:52278149-52278585	Hela-S3	cervix:	n/a	n/a
41	FOS	chr3:52278098-52278678	HUVEC	blood vessel:	n/a	chr3:52278232-52278240 chr3:52278231-52278241 chr3:52278504-52278514 chr3:52278233-52278240 chr3:52278231-52278241 chr3:52278232-52278240 chr3:52278503-52278515 chr3:52278231-52278241 chr3:52278504-52278514 chr3:52278231-52278241
42	BATF	chr3:52277944-52278754	GM12878	blood:	n/a	chr3:52278229-52278239
43	EBF1	chr3:52277812-52280262	GM12878	blood:	n/a	n/a
44	SPI1	chr3:52278176-52278752	GM12891	blood:	n/a	chr3:52278471-52278484
45	POLR2A	chr3:52278169-52278489	GM12878	blood:	n/a	n/a
46	POLR2A	chr3:52278021-52280334	GM12892	blood:	n/a	n/a
47	CHD1	chr3:52277999-52278571	GM12878	blood:	n/a	n/a
48	POLR2A	chr3:52277967-52278505	Hela-S3	cervix:	n/a	n/a
49	PML	chr3:52277831-52279574	GM12878	blood:	n/a	chr3:52278233-52278242
50	BCL3	chr3:52278017-52278711	GM12878	blood:	n/a	chr3:52278231-52278240

No.	Distal block	Cell Line	Cell type
1	chr3:52278055..52281861-chr3:52310588..52314481,6	K562	blood:
2	chr3:52278055..52281861-chr3:52310505..52315451,9	K562	blood:
3	chr3:52277680..52279387-chr3:52372909..52375320,2	K562	blood:
4	chr3:52277093..52279461-chr3:52290667..52292256,2	MCF-7	breast:
5	chr3:52278070..52281652-chr3:52320199..52323338,4	MCF-7	breast:

Variant related genes	Relation type
TWF2	TF binding region
PPM1M	TF binding region
ENSG00000168237	Chromatin interaction
ENSG00000164091	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10460962	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10461027	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes]
rs10461028	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11706515	1.00[CEU][hapmap];0.88[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs11706541	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11707056	1.00[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.97[EUR][1000 genomes]
rs11708581	0.91[CEU][hapmap];0.88[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs11708811	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs11710014	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11711914	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11711974	1.00[CEU][hapmap];0.88[GIH][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11713464	0.86[AMR][1000 genomes]
rs11713914	1.00[CEU][hapmap];0.88[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs11714358	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11715208	0.97[EUR][1000 genomes]
rs11715382	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11715391	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11716487	1.00[CEU][hapmap];0.88[TSI][hapmap]
rs11717028	0.94[EUR][1000 genomes]
rs11718125	0.81[LWK][hapmap]
rs11718729	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11719760	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11720365	1.00[CEU][hapmap];0.88[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs11721277	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13075370	0.85[LWK][hapmap]
rs17052051	1.00[CEU][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17052052	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17052053	0.91[CEU][hapmap];0.85[MEX][hapmap];0.96[TSI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17052054	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1767	0.91[CEU][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1769	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35976326	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3733063	0.89[ASW][hapmap];0.91[CEU][hapmap];0.85[LWK][hapmap];0.98[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3886875	1.00[CEU][hapmap];0.88[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.85[EUR][1000 genomes]
rs4082828	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55676974	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55806905	0.91[EUR][1000 genomes]
rs55813842	0.91[EUR][1000 genomes]
rs55847657	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56002041	0.91[EUR][1000 genomes]
rs56322342	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56352611	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56899118	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs57849650	0.91[EUR][1000 genomes]
rs58531656	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58879205	0.86[AMR][1000 genomes]
rs60382084	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61644644	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6445385	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6783652	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6793317	0.91[CEU][hapmap];0.88[LWK][hapmap];0.85[MEX][hapmap];0.96[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6809248	0.96[YRI][hapmap];0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73072990	0.85[EUR][1000 genomes]
rs73088773	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73088783	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73088785	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73088791	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73088800	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73091166	0.91[EUR][1000 genomes]
rs73091168	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs746239	0.91[EUR][1000 genomes]
rs7615405	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7628461	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7633687	1.00[CEU][hapmap];0.88[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs7643913	0.86[CEU][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519445	chr3:52004317-52367932	Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS 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 miRNA target site	134 gene(s)	inside rSNPs	diseases
2	nsv984541	chr3:52055970-52285682	Genic enhancers Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv470572	chr3:52123313-52350212	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	103 gene(s)	inside rSNPs	diseases
4	nsv460537	chr3:52148233-52290550	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
5	nsv590301	chr3:52148233-52290550	Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
6	nsv508218	chr3:52155869-52290410	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv834694	chr3:52178983-52335821	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	102 gene(s)	inside rSNPs	diseases
8	nsv834695	chr3:52199701-52400577	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	98 gene(s)	inside rSNPs	diseases
9	nsv876787	chr3:52236762-52367932	Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	90 gene(s)	inside rSNPs	diseases
10	nsv876788	chr3:52247110-52367932	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	90 gene(s)	inside rSNPs	diseases
11	nsv876789	chr3:52247110-52575831	Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
12	nsv876790	chr3:52261382-52286825	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
13	nsv876791	chr3:52269491-52286825	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription 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	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs7638204	NISCH	cis	parietal	SCAN
rs7638204	SEMA3G	cis	cerebellum	SCAN
rs7638204	ZNF589	cis	cerebellum	SCAN
rs7638204	DNAH1	cis	parietal	SCAN
rs7638204	MST1	cis	parietal	SCAN
rs7638204	PPM1M	cis	parietal	SCAN
rs7638204	DNAH1	cis	cerebellum	SCAN
rs7638204	TKT	cis	cerebellum	SCAN
rs7638204	PPM1M	cis	Artery Tibial	GTEx

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52274400-52278800	Weak transcription	Fetal Lung	lung
2	chr3:52274400-52279000	Weak transcription	Fetal Heart	heart
3	chr3:52274400-52279400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:52274600-52278400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr3:52274600-52279000	Weak transcription	Brain Anterior Caudate	brain
6	chr3:52274600-52279000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr3:52274800-52278600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr3:52274800-52278800	Weak transcription	Colon Smooth Muscle	Colon
9	chr3:52274800-52279200	Weak transcription	Liver	Liver
10	chr3:52274800-52279200	Weak transcription	Pancreas	Pancrea
11	chr3:52274800-52279200	Weak transcription	Right Atrium	heart
12	chr3:52275000-52278800	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr3:52275000-52279000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr3:52275000-52279200	Weak transcription	Stomach Mucosa	stomach
15	chr3:52275200-52278400	Weak transcription	NHLF	lung
16	chr3:52275200-52279000	Weak transcription	Brain Hippocampus Middle	brain
17	chr3:52275200-52279000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr3:52275200-52279000	Weak transcription	Brain Substantia Nigra	brain
19	chr3:52275200-52279000	Weak transcription	A549	lung
20	chr3:52275200-52279200	Weak transcription	HSMM	muscle
21	chr3:52275200-52279400	Weak transcription	Brain Angular Gyrus	brain
22	chr3:52275400-52278400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr3:52275400-52278400	Weak transcription	Thymus	Thymus
24	chr3:52275400-52279000	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr3:52276600-52279000	Weak transcription	K562	blood
26	chr3:52277200-52278800	Enhancers	Primary B cells from cord blood	blood
27	chr3:52277400-52279000	Enhancers	Primary B cells from peripheral blood	blood
28	chr3:52277400-52279000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr3:52277600-52278400	Enhancers	Primary T cells fromperipheralblood	blood
30	chr3:52277600-52278400	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr3:52277600-52278400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr3:52277600-52278800	Enhancers	Primary T cells from cord blood	blood
33	chr3:52277600-52278800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr3:52277600-52278800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr3:52277600-52278800	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr3:52277600-52278800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr3:52277600-52279000	Enhancers	Primary hematopoietic stem cells	blood
38	chr3:52277600-52279000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr3:52277600-52279000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr3:52277600-52279000	Enhancers	Placenta	Placenta
41	chr3:52277600-52279000	Enhancers	Spleen	Spleen
42	chr3:52277600-52279200	Enhancers	HUVEC	blood vessel
43	chr3:52277600-52279400	Enhancers	Lung	lung
44	chr3:52277600-52279600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:52277600-52279600	Enhancers	HMEC	breast
46	chr3:52277600-52282000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr3:52277800-52278400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr3:52277800-52278600	Flanking Active TSS	GM12878-XiMat	blood
49	chr3:52277800-52278800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:52277800-52279000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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