Variant report

Variant	rs2297226
Chromosome Location	chr1:186343759-186343760
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:115)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:115 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:186343484-186346756	MCF10A-Er-Src	breast:	n/a	n/a
2	TCF7L2	chr1:186343626-186345385	Hela-S3	cervix:	n/a	chr1:186343834-186343841
3	PML	chr1:186343478-186345433	GM12878	blood:	n/a	n/a
4	MAZ	chr1:186343570-186345389	K562	blood:	n/a	n/a
5	POLR2A	chr1:186343537-186345335	NB4	blood:	n/a	n/a
6	TBP	chr1:186343433-186345520	Hela-S3	cervix:	n/a	n/a
7	JUND	chr1:186343365-186345433	K562	blood:	n/a	chr1:186344583-186344592
8	JUND	chr1:186343749-186345480	H1-hESC	embryonic stem cell:	n/a	chr1:186344583-186344592
9	POLR2A	chr1:186343407-186345626	K562	blood:	n/a	n/a
10	E2F4	chr1:186343529-186345366	K562	blood:	n/a	chr1:186344810-186344821 chr1:186344824-186344833 chr1:186344810-186344821
11	POLR2A	chr1:186343447-186345545	K562	blood:	n/a	n/a
12	FOXA1	chr1:186343368-186343786	HepG2	liver:	n/a	n/a
13	RCOR1	chr1:186343541-186345452	K562	blood:	n/a	n/a
14	POLR2A	chr1:186343618-186345305	GM12892	blood:	n/a	n/a
15	POLR2A	chr1:186343483-186345387	Hela-S3	cervix:	n/a	n/a
16	RCOR1	chr1:186343610-186345431	Hela-S3	cervix:	n/a	n/a
17	ELF1	chr1:186343594-186345384	MCF-7	breast:	n/a	n/a
18	NFIC	chr1:186343734-186344469	HepG2	liver:	n/a	n/a
19	RCOR1	chr1:186343549-186345294	K562	blood:	n/a	n/a
20	MYC	chr1:186343499-186345841	K562	blood:	n/a	n/a
21	CUX1	chr1:186343439-186345835	K562	blood:	n/a	n/a
22	POLR2A	chr1:186343606-186345330	GM19099	blood:	n/a	n/a
23	MXI1	chr1:186343481-186345385	Hela-S3	cervix:	n/a	chr1:186344905-186344914
24	TAF1	chr1:186343535-186345418	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr1:186343584-186343847	MCF-7	breast:	n/a	n/a
26	HA-E2F1	chr1:186343493-186345378	MCF-7	breast:	n/a	chr1:186344810-186344821 chr1:186344824-186344833 chr1:186344810-186344821
27	MAFK	chr1:186343525-186345239	K562	blood:	n/a	n/a
28	NFYB	chr1:186343388-186345006	K562	blood:	n/a	n/a
29	RUNX3	chr1:186343519-186345355	GM12878	blood:	n/a	chr1:186344615-186344630
30	POLR2A	chr1:186343500-186345385	GM18505	blood:	n/a	n/a
31	POLR2A	chr1:186343555-186345386	GM18526	blood:	n/a	n/a
32	TBP	chr1:186343532-186345373	K562	blood:	n/a	n/a
33	SIN3AK20	chr1:186343479-186345294	K562	blood:	n/a	n/a
34	POLR2A	chr1:186343505-186345376	K562	blood:	n/a	n/a
35	PML	chr1:186343442-186345447	K562	blood:	n/a	n/a
36	IRF1	chr1:186342945-186345414	K562	blood:	n/a	chr1:186344937-186344946 chr1:186344823-186344837 chr1:186343899-186343908
37	TBL1XR1	chr1:186343518-186345293	K562	blood:	n/a	n/a
38	USF2	chr1:186343510-186344180	GM12878	blood:	n/a	n/a
39	MXI1	chr1:186343505-186345395	GM12878	blood:	n/a	chr1:186344905-186344914
40	MYC	chr1:186343550-186343815	MCF10A-Er-Src	breast:	n/a	n/a
41	TBL1XR1	chr1:186343214-186345266	K562	blood:	n/a	n/a
42	RELA	chr1:186343486-186345373	GM18951	blood:	n/a	n/a
43	MYC	chr1:186343512-186345390	NB4	blood:	n/a	n/a
44	RELA	chr1:186343753-186345191	GM19099	blood:	n/a	n/a
45	POLR2A	chr1:186343446-186345357	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr1:186343534-186345345	GM15510	blood:	n/a	n/a
47	ARID3A	chr1:186343326-186343808	K562	blood:	n/a	n/a
48	MAZ	chr1:186343552-186345397	IMR90	lung:	n/a	n/a
49	POLR2A	chr1:186343600-186345393	GM19193	blood:	n/a	n/a
50	SIN3AK20	chr1:186343294-186345431	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:186343755-186343805	HL-60	blood:	n/a
2	chr1:186343755-186343805	HepG2	liver:	n/a
3	chr1:186343755-186343805	HEK293	kidney:	embryo
4	chr1:186343755-186343805	MCF10A-Er-Src	breast:	n/a
5	chr1:186343755-186343805	HRE	kidney:	n/a
6	chr1:186343755-186343805	BJ	skin:	n/a
7	chr1:186343755-186343805	AG09309	skin:	n/a
8	chr1:186343755-186343805	HCM	heart:	n/a
9	chr1:186343755-186343805	LNCaP	prostate:	n/a
10	chr1:186343755-186343805	ECC-1	luminal epithelium:	n/a
11	chr1:186343755-186343805	AG10803	skin:	n/a
12	chr1:186343755-186343805	HMEC	breast:	n/a
13	chr1:186343755-186343805	NH-A	brain:	n/a
14	chr1:186343755-186343805	ovcar-3	ovarian:	n/a
15	chr1:186343755-186343805	AoSMC	blood vessel:	n/a
16	chr1:186343755-186343805	NT2-D1	testis:	n/a
17	chr1:186343755-186343805	HRPEpiC	eye:	n/a
18	chr1:186343755-186343805	H1-hESC	embryonic stem cell:	embryo
19	chr1:186343755-186343805	PFSK-1	brain:	n/a
20	chr1:186343755-186343805	HUVEC	blood vessel:	n/a
21	chr1:186343755-186343805	T-47D	breast:	n/a
22	chr1:186343755-186343805	PANC-1	pancreas:	n/a
23	chr1:186343755-186343805	HAEpiC	amniotic membrane:	n/a
24	chr1:186343755-186343805	HCF	heart:	n/a
25	chr1:186343755-186343805	SK-N-SH	brain:	n/a
26	chr1:186343755-186343805	IMR90	lung:	fetal
27	chr1:186343755-186343805	AG04449	skin:	fetal
28	chr1:186343755-186343805	A549	lung:	n/a
29	chr1:186343755-186343805	HRCEpiC	kidney:	n/a
30	chr1:186343755-186343805	RPTEC	kidney:	n/a
31	chr1:186343755-186343805	HIPEpiC	eye:	n/a
32	chr1:186343755-186343805	NHDF-neo	bronchial:	n/a
33	chr1:186343755-186343805	NB4	blood:	n/a
34	chr1:186343755-186343805	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:186343755-186343805	NHBE	bronchial:	n/a
36	chr1:186343755-186343805	Caco-2	colon:	n/a
37	chr1:186343755-186343805	GM12892	blood:	n/a
38	chr1:186343755-186343805	SK-N-MC	brain:	n/a
39	chr1:186343755-186343805	SKMC	muscle:	n/a
40	chr1:186343755-186343805	GM12891	blood:	n/a
41	chr1:186343755-186343805	BE2_C	brain:	n/a
42	chr1:186343755-186343805	HNPCEpiC	eye:	n/a
43	chr1:186343755-186343805	ProgFib	skin:	n/a
44	chr1:186343755-186343805	HCPEpiC	choroid plexus:	n/a
45	chr1:186343755-186343805	AG04450	lung:	fetal
46	chr1:186343755-186343805	K562	blood:	n/a
47	chr1:186343755-186343805	Jurkat	blood:	n/a
48	chr1:186343755-186343805	PrEC	prostate:	n/a
49	chr1:186343755-186343805	U87	brain:	n/a
50	chr1:186343755-186343805	GM12878	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:186343585..186344319-chr12:49658423..49658946,2	Hela-S3	cervix:
2	chr1:186279942..186281845-chr1:186343325..186346234,2	K562	blood:
3	chr1:186290710..186293581-chr1:186342428..186344666,2	K562	blood:
4	chr1:186341227..186346056-chr1:193025925..193030298,4	K562	blood:
5	chr1:186311436..186314433-chr1:186341934..186345376,3	K562	blood:
6	chr1:186312933..186317180-chr1:186341100..186346147,6	K562	blood:
7	chr1:186291321..186293772-chr1:186343182..186344896,2	MCF-7	breast:

No data

Variant related genes	Relation type
C1orf27	TF binding region
C1orf27	CpG island
ENSG00000238754	Chromatin interaction
ENSG00000167553	Chromatin interaction
ENSG00000202025	Chromatin interaction
ENSG00000258101	Chromatin interaction
ENSG00000047410	Chromatin interaction
ENSG00000116747	Chromatin interaction
ENSG00000116750	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 5 )

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

rs_ID	r²[population]
rs10494583	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10494584	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.86[ASN][1000 genomes]
rs1406294	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs16825150	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs16825183	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16825185	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16825201	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16825224	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16825230	0.88[YRI][hapmap];0.81[AFR][1000 genomes]
rs16825243	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16825248	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16825279	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16825335	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17491733	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1919199	0.83[ASN][1000 genomes]
rs1919200	0.81[ASN][1000 genomes]
rs2272412	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2273777	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2273778	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs28715477	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3119331	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs3131554	0.82[CHB][hapmap];0.90[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap]
rs34585917	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3736595	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3736597	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3753565	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3766699	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3766702	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3766703	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3766704	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3766705	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3766707	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3820181	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3820182	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs57040195	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6425024	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6425027	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425028	0.94[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6664763	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6667940	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6678193	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6679066	0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6689129	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7514615	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7525634	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7556543	0.92[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004481	chr1:186095854-186750968	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv535223	chr1:186095854-186750968	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv548399	chr1:186295930-186353461	Bivalent/Poised TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
4	esv1822818	chr1:186301447-186441585	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS 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 target site	29 gene(s)	inside rSNPs	diseases
5	nsv1012164	chr1:186323867-186565995	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	esv2762201	chr1:186323879-186566007	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs2297226	CACNA1E	cis	cerebellum	SCAN
rs2297226	C1orf27	cis	cerebellum	SCAN
rs2297226	OCLM	cis	parietal	SCAN
rs2297226	OCLM	cis	cerebellum	SCAN
rs2297226	C1orf27	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186335200-186343800	Weak transcription	Spleen	Spleen
2	chr1:186342200-186346600	Active TSS	NHLF	lung
3	chr1:186342400-186343800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:186342400-186343800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:186342400-186344000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:186342400-186345800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:186342400-186346000	Active TSS	Fetal Kidney	kidney
8	chr1:186342400-186346400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr1:186342600-186343800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:186342600-186344200	Flanking Active TSS	Primary B cells from cord blood	blood
11	chr1:186342600-186344200	Active TSS	Brain Germinal Matrix	brain
12	chr1:186342600-186345800	Active TSS	Breast Myoepithelial Primary Cells	Breast
13	chr1:186342600-186345800	Active TSS	NH-A	brain
14	chr1:186342600-186346000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:186342600-186346000	Active TSS	K562	blood
16	chr1:186342600-186346400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:186342600-186346400	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr1:186342800-186343800	Flanking Active TSS	Stomach Smooth Muscle	stomach
19	chr1:186342800-186345800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr1:186342800-186346000	Active TSS	Fetal Brain Female	brain
21	chr1:186342800-186346000	Active TSS	Fetal Stomach	stomach
22	chr1:186342800-186346000	Active TSS	HMEC	breast
23	chr1:186342800-186346000	Active TSS	NHDF-Ad	bronchial
24	chr1:186342800-186346200	Active TSS	A549	lung
25	chr1:186342800-186346400	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr1:186342800-186349000	Active TSS	GM12878-XiMat	blood
27	chr1:186343000-186343800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
28	chr1:186343000-186343800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr1:186343000-186343800	Flanking Active TSS	Liver	Liver
30	chr1:186343000-186343800	Flanking Active TSS	Brain Angular Gyrus	brain
31	chr1:186343000-186343800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr1:186343000-186344000	Flanking Active TSS	Primary T cells from cord blood	blood
33	chr1:186343000-186344000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
34	chr1:186343000-186344200	Active TSS	Right Atrium	heart
35	chr1:186343000-186345400	ZNF genes & repeats	Fetal Brain Male	brain
36	chr1:186343000-186345800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr1:186343000-186345800	Active TSS	Fetal Intestine Large	intestine
38	chr1:186343000-186345800	Active TSS	Fetal Thymus	thymus
39	chr1:186343000-186345800	Active TSS	Hela-S3	cervix
40	chr1:186343000-186346000	Active TSS	H1 Cell Line	embryonic stem cell
41	chr1:186343000-186346000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr1:186343000-186346000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:186343000-186346000	Active TSS	Fetal Muscle Leg	muscle
44	chr1:186343000-186346000	Active TSS	Psoas Muscle	Psoas
45	chr1:186343000-186346400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr1:186343200-186343800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr1:186343200-186343800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr1:186343200-186343800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr1:186343200-186343800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
50	chr1:186343200-186344000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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