Variant report

Variant	rs587553
Chromosome Location	chr3:121265913-121265914
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	CEBPB	chr3:121264767-121265991	A549	lung:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
2	RAD21	chr3:121265429-121265970	ECC-1	luminal epithelium:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
3	CTCF	chr3:121264809-121265939	GM12878	blood:	n/a	chr3:121265701-121265719 chr3:121265703-121265724 chr3:121265702-121265718
4	SIX5	chr3:121264551-121266074	A549	lung:	n/a	n/a
5	MXI1	chr3:121263658-121266103	IMR90	lung:	n/a	n/a
6	ARID3A	chr3:121265453-121265941	HepG2	liver:	n/a	n/a
7	ZNF143	chr3:121265552-121265924	K562	blood:	n/a	n/a
8	FOXA1	chr3:121265520-121265947	HepG2	liver:	n/a	n/a
9	CTCF	chr3:121265541-121265923	H1-hESC	embryonic stem cell:	n/a	chr3:121265701-121265719 chr3:121265703-121265724 chr3:121265702-121265718
10	CEBPB	chr3:121265352-121265933	HepG2	liver:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
11	RAD21	chr3:121264782-121265968	IMR90	lung:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
12	TEAD4	chr3:121265460-121265966	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:121264621-121266051	GM12878	blood:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
14	RAD21	chr3:121265550-121265924	K562	blood:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
15	CEBPB	chr3:121264666-121266054	MCF-7	breast:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
16	CEBPB	chr3:121265292-121265994	K562	blood:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
17	HCFC1	chr3:121264036-121266047	Hela-S3	cervix:	n/a	n/a
18	GTF2F1	chr3:121264677-121265941	Hela-S3	cervix:	n/a	n/a
19	GABPA	chr3:121264238-121265938	A549	lung:	n/a	chr3:121264842-121264851
20	YY1	chr3:121265607-121265931	HCT-116	colon:	n/a	n/a
21	CEBPB	chr3:121264724-121265949	HepG2	liver:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
22	EP300	chr3:121265672-121265928	K562	blood:	n/a	n/a
23	CTCF	chr3:121265521-121265984	MCF-7	breast:	n/a	chr3:121265701-121265719 chr3:121265703-121265724 chr3:121265702-121265718
24	RAD21	chr3:121264604-121266123	SK-N-SH	brain:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
25	RAD21	chr3:121265441-121265946	HepG2	liver:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
26	CTCF	chr3:121265269-121266020	HCT-116	colon:	n/a	chr3:121265701-121265719 chr3:121265703-121265724 chr3:121265702-121265718
27	MAX	chr3:121264156-121265942	NB4	blood:	n/a	chr3:121264347-121264355 chr3:121264534-121264544
28	RAD21	chr3:121265404-121265989	HCT-116	colon:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
29	CTCF	chr3:121265438-121265979	MCF-7	breast:	n/a	chr3:121265701-121265719 chr3:121265703-121265724 chr3:121265702-121265718
30	RAD21	chr3:121265361-121265946	GM12878	blood:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
31	RAD21	chr3:121265469-121265982	MCF-7	breast:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
32	RAD21	chr3:121265536-121265948	GM12878	blood:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
33	ZNF384	chr3:121265508-121265919	GM12878	blood:	n/a	n/a
34	RAD21	chr3:121265472-121265938	SK-N-SH_RA	brain:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
35	PML	chr3:121264311-121266009	GM12878	blood:	n/a	n/a
36	CEBPB	chr3:121265317-121265984	HCT-116	colon:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
37	CEBPB	chr3:121264701-121265949	A549	lung:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
38	CTCF	chr3:121264888-121265989	K562	blood:	n/a	chr3:121265701-121265719 chr3:121265703-121265724 chr3:121265702-121265718
39	FOXA1	chr3:121265591-121265991	HepG2	liver:	n/a	n/a
40	RAD21	chr3:121264454-121266043	HCT-116	colon:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
41	CEBPB	chr3:121265309-121265961	H1-hESC	embryonic stem cell:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
42	RAD21	chr3:121265508-121266049	MCF-7	breast:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
43	CEBPB	chr3:121264670-121266056	A549	lung:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
44	RAD21	chr3:121265387-121266094	A549	lung:	n/a	chr3:121265702-121265721 chr3:121265706-121265715
45	MXI1	chr3:121263660-121266065	SK-N-SH	brain:	n/a	n/a
46	FOXM1	chr3:121265422-121266017	GM12878	blood:	n/a	n/a
47	MTA3	chr3:121264006-121265993	GM12878	blood:	n/a	n/a
48	CEBPB	chr3:121265347-121265933	HepG2	liver:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
49	CTCF	chr3:121264831-121265933	IMR90	lung:	n/a	chr3:121265701-121265719 chr3:121265703-121265724 chr3:121265702-121265718
50	SMC3	chr3:121265449-121265939	HepG2	liver:	n/a	chr3:121265703-121265717

No.	Distal block	Cell Line	Cell type
1	chr3:121264864..121267091-chr3:122101354..122103102,2	MCF-7	breast:
2	chr3:121263813..121266298-chr3:122398939..122401596,2	K562	blood:
3	chr3:121265150..121267222-chr3:121267374..121269393,2	K562	blood:
4	chr3:121264298..121266034-chr3:122100794..122102974,2	MCF-7	breast:
5	chr3:121265303..121265930-chr3:121811130..121811872,2	MCF-7	breast:
6	chr3:121264839..121267237-chr3:122281910..122284575,2	MCF-7	breast:
7	chr3:121265697..121266207-chr3:122977401..122978341,2	K562	blood:

Variant related genes	Relation type
POLQ	TF binding region
ENSG00000114023	Chromatin interaction
ENSG00000173193	Chromatin interaction
ENSG00000160124	Chromatin interaction
ENSG00000163840	Chromatin interaction
ENSG00000138496	Chromatin interaction

Extended variants
information (count: 105 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10451895	0.85[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10934551	0.85[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11706583	0.96[ASN][1000 genomes]
rs11709378	0.95[ASN][1000 genomes]
rs11709726	1.00[JPT][hapmap]
rs11711667	0.89[ASN][1000 genomes]
rs11713643	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11714746	0.98[ASN][1000 genomes]
rs11714774	1.00[ASN][1000 genomes]
rs11718918	0.89[ASN][1000 genomes]
rs12488196	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12496163	0.86[ASN][1000 genomes]
rs12632308	0.89[ASN][1000 genomes]
rs12634017	0.81[ASN][1000 genomes]
rs12635218	0.89[ASN][1000 genomes]
rs13059229	0.85[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs13065220	1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap]
rs13077237	0.90[ASN][1000 genomes]
rs13077305	1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs13080007	0.89[ASN][1000 genomes]
rs13082118	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs13085365	0.96[ASN][1000 genomes]
rs13095550	0.90[ASN][1000 genomes]
rs13097659	0.85[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs13100579	0.98[ASN][1000 genomes]
rs1381057	1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap]
rs1381058	0.94[CHD][hapmap];1.00[JPT][hapmap]
rs1381059	0.85[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1877968	0.95[ASN][1000 genomes]
rs1877969	0.95[ASN][1000 genomes]
rs1987098	0.82[EUR][1000 genomes]
rs2030531	0.85[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs2126139	0.80[EUR][1000 genomes]
rs2127024	0.80[EUR][1000 genomes]
rs2169301	0.96[ASN][1000 genomes]
rs2331962	0.96[ASN][1000 genomes]
rs28406368	0.89[ASN][1000 genomes]
rs3101345	0.88[CEU][hapmap]
rs3218649	0.85[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs3732406	0.94[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs3772122	0.85[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs3772124	0.91[ASN][1000 genomes]
rs3806614	0.85[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs3845860	0.91[ASN][1000 genomes]
rs3845863	0.91[ASN][1000 genomes]
rs3911713	0.85[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4555467	0.85[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4676677	1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap]
rs4676680	0.88[ASN][1000 genomes]
rs4676728	0.95[ASN][1000 genomes]
rs488636	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs500100	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs500103	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs502643	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs513380	0.89[EUR][1000 genomes]
rs524026	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs541818	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs575913	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61796946	0.86[ASN][1000 genomes]
rs6438630	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6438633	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs66922316	0.91[ASN][1000 genomes]
rs6769377	0.85[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs6778684	0.89[ASN][1000 genomes]
rs6782025	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.81[EUR][1000 genomes]
rs6782033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.81[EUR][1000 genomes]
rs6784324	0.88[ASN][1000 genomes]
rs6787048	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.80[EUR][1000 genomes]
rs6793252	1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs6797376	0.85[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs6797682	0.96[ASN][1000 genomes]
rs6798699	0.87[CHD][hapmap];1.00[JPT][hapmap]
rs6806191	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs693403	1.00[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];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs702019	1.00[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];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7609781	0.82[EUR][1000 genomes]
rs7612018	0.85[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7615529	0.85[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7617748	0.96[ASN][1000 genomes]
rs7621376	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs7622867	0.85[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7622881	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7622897	0.89[ASN][1000 genomes]
rs7627978	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7628081	0.98[ASN][1000 genomes]
rs7632907	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.81[EUR][1000 genomes]
rs7633930	1.00[CHB][hapmap];0.88[JPT][hapmap];0.98[ASN][1000 genomes]
rs7634611	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7645027	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs7645050	0.96[ASN][1000 genomes]
rs7650658	0.82[EUR][1000 genomes]
rs9849118	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs9863608	0.83[TSI][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	nsv998555	chr3:120700604-121348015	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
2	nsv591395	chr3:120970900-121501070	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv591396	chr3:120970900-121557533	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv591397	chr3:120977383-121505882	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv591400	chr3:121070299-121339354	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv999335	chr3:121100283-121408766	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv877381	chr3:121192350-121343500	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv1007522	chr3:121200563-121374051	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv999349	chr3:121253990-121360206	Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	esv3445327	chr3:121260311-121288302	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
11	esv2757006	chr3:121264886-121323465	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	esv2759172	chr3:121264886-121323465	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs587553	CHST13	cis	parietal	SCAN

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121263800-121266000	Active TSS	Fetal Kidney	kidney
2	chr3:121263800-121266000	Active TSS	A549	lung
3	chr3:121264200-121266000	Flanking Active TSS	Liver	Liver
4	chr3:121264800-121266000	Active TSS	Brain Anterior Caudate	brain
5	chr3:121265600-121266000	Enhancers	Pancreas	Pancrea
6	chr3:121265600-121266000	Enhancers	Small Intestine	intestine
7	chr3:121265600-121266200	Active TSS	HepG2	liver
8	chr3:121265600-121267200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr3:121265600-121267200	Weak transcription	Stomach Mucosa	stomach
10	chr3:121265600-121271000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr3:121265800-121266000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:121265800-121266000	Enhancers	Primary B cells from cord blood	blood
13	chr3:121265800-121266000	Active TSS	Primary hematopoietic stem cells short term culture	blood
14	chr3:121265800-121266000	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr3:121265800-121266000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr3:121265800-121266000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr3:121265800-121266000	Enhancers	Placenta	Placenta
18	chr3:121265800-121266000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr3:121265800-121266000	Flanking Active TSS	Rectal Smooth Muscle	rectum
20	chr3:121265800-121266000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
21	chr3:121265800-121266000	Enhancers	Dnd41	blood
22	chr3:121265800-121266000	Enhancers	NHLF	lung
23	chr3:121265800-121266000	Enhancers	Osteobl	bone
24	chr3:121265800-121266200	Enhancers	Primary T cells fromperipheralblood	blood
25	chr3:121265800-121266400	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr3:121265800-121267200	Weak transcription	Primary B cells from peripheral blood	blood
27	chr3:121265800-121267200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr3:121265800-121267200	Weak transcription	Duodenum Mucosa	Duodenum
29	chr3:121265800-121267200	Weak transcription	Fetal Intestine Large	intestine
30	chr3:121265800-121267200	Weak transcription	Fetal Intestine Small	intestine
31	chr3:121265800-121267200	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr3:121265800-121267200	Weak transcription	HMEC	breast
33	chr3:121265800-121267200	Weak transcription	NHEK	skin
34	chr3:121265800-121267400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:121265800-121267400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr3:121265800-121267800	Enhancers	GM12878-XiMat	blood
37	chr3:121265800-121268600	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr3:121265800-121269200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr3:121265800-121269200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr3:121265800-121270600	Weak transcription	Fetal Lung	lung
41	chr3:121265800-121270800	Weak transcription	K562	blood
42	chr3:121265800-121271200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr3:121265800-121271200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:121265800-121271400	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr3:121265800-121280600	Weak transcription	H1 Cell Line	embryonic stem cell

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