Variant report

Variant	rs11130124
Chromosome Location	chr3:47292183-47292184
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:169)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:169 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ELF1	chr3:47292007-47292347	HepG2	liver:	n/a	n/a
2	HCFC1	chr3:47292144-47292414	K562	blood:	n/a	n/a
3	SMC3	chr3:47291996-47292617	SK-N-SH	brain:	n/a	n/a
4	CTCF	chr3:47292126-47292421	Lung_OC	lung:	n/a	n/a
5	RAD21	chr3:47292090-47292451	K562	blood:	n/a	n/a
6	CTCF	chr3:47292179-47292355	GM13976	blood:	n/a	n/a
7	MAZ	chr3:47292013-47292482	K562	blood:	n/a	chr3:47292390-47292401
8	SMC3	chr3:47292059-47292514	K562	blood:	n/a	n/a
9	CTCF	chr3:47292160-47292310	AG04449	skin:	n/a	n/a
10	JUND	chr3:47292078-47292476	K562	blood:	n/a	n/a
11	CTCF	chr3:47292176-47292440	GM19239	blood:	n/a	n/a
12	CTCF	chr3:47292165-47292391	T-47D	breast:	n/a	n/a
13	RAD21	chr3:47292020-47292539	H1-hESC	embryonic stem cell:	n/a	n/a
14	EP300	chr3:47292106-47292451	K562	blood:	n/a	chr3:47292122-47292129
15	CTCF	chr3:47292160-47292310	WI-38	lung:	n/a	n/a
16	CTCF	chr3:47292079-47292457	A549	lung:	n/a	n/a
17	CTCF	chr3:47292180-47292330	HAc	cerebellar:	n/a	n/a
18	CTCF	chr3:47292140-47292290	HFF	foreskin:	n/a	n/a
19	RAD21	chr3:47292082-47292504	MCF-7	breast:	n/a	n/a
20	CTCF	chr3:47292180-47292330	AoAF	blood vessel:	n/a	n/a
21	MYC	chr3:47292098-47292399	K562	blood:	n/a	n/a
22	CTCF	chr3:47292160-47292310	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr3:47292065-47292478	GM12878	blood:	n/a	n/a
24	CTCF	chr3:47291958-47292562	K562	blood:	n/a	n/a
25	RAD21	chr3:47292112-47292456	K562	blood:	n/a	n/a
26	CTCF	chr3:47292167-47292427	GM12892	blood:	n/a	n/a
27	ZNF143	chr3:47292138-47292461	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr3:47292161-47292379	MCF-7	breast:	n/a	n/a
29	RAD21	chr3:47292051-47292490	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr3:47292093-47292409	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr3:47292073-47292441	MCF-7	breast:	n/a	n/a
32	CTCF	chr3:47292140-47292290	MCF-7	breast:	n/a	n/a
33	ARID3A	chr3:47292083-47292283	HepG2	liver:	n/a	n/a
34	ZNF143	chr3:47292121-47292451	K562	blood:	n/a	n/a
35	RAD21	chr3:47292060-47292524	A549	lung:	n/a	n/a
36	CTCF	chr3:47292162-47292435	GM19240	blood:	n/a	n/a
37	CTCF	chr3:47292175-47292363	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr3:47292160-47292373	LNCaP	prostate:	n/a	n/a
39	CTCF	chr3:47292160-47292310	HRPEpiC	eye:	n/a	n/a
40	RAD21	chr3:47292130-47292436	A549	lung:	n/a	n/a
41	CTCF	chr3:47292108-47292383	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr3:47291852-47292637	SK-N-SH	brain:	n/a	n/a
43	MAZ	chr3:47292172-47292358	Hela-S3	cervix:	n/a	n/a
44	ELF1	chr3:47292133-47292417	HepG2	liver:	n/a	n/a
45	CTCF	chr3:47292173-47292362	GM10248	blood:	n/a	n/a
46	CTCF	chr3:47292160-47292310	HL-60	blood:	n/a	n/a
47	CTCF	chr3:47292182-47292396	A549	lung:	n/a	n/a
48	CTCF	chr3:47292180-47292330	GM12873	blood:	n/a	n/a
49	CTCF	chr3:47292180-47292330	HPF	lung:	n/a	n/a
50	TBL1XR1	chr3:47292163-47292530	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:47292165-47292215	HRE	kidney:	n/a
2	chr3:47292165-47292215	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:47292165-47292215	HMEC	breast:	n/a
4	chr3:47292165-47292215	HCPEpiC	choroid plexus:	n/a
5	chr3:47292165-47292215	HEK293	kidney:	embryo
6	chr3:47292165-47292215	GM12878	blood:	n/a
7	chr3:47292165-47292215	MCF10A-Er-Src	breast:	n/a
8	chr3:47292165-47292215	HCM	heart:	n/a
9	chr3:47292165-47292215	T-47D	breast:	n/a
10	chr3:47292165-47292215	BE2_C	brain:	n/a
11	chr3:47292165-47292215	AG09319	gingival:	n/a
12	chr3:47292165-47292215	SAEC	small airway:	n/a
13	chr3:47292165-47292215	ProgFib	skin:	n/a
14	chr3:47292165-47292215	HRPEpiC	eye:	n/a
15	chr3:47292165-47292215	GM12891	blood:	n/a
16	chr3:47292165-47292215	CMK	blood:	n/a
17	chr3:47292165-47292215	HUVEC	blood vessel:	n/a
18	chr3:47292165-47292215	Jurkat	blood:	n/a
19	chr3:47292165-47292215	SKMC	muscle:	n/a
20	chr3:47292165-47292215	SK-N-SH_RA	brain:	n/a
21	chr3:47292165-47292215	BJ	skin:	n/a
22	chr3:47292165-47292215	GM06990	blood:	n/a
23	chr3:47292165-47292215	NT2-D1	testis:	n/a
24	chr3:47292165-47292215	ECC-1	luminal epithelium:	n/a
25	chr3:47292165-47292215	HEEpiC	esophagus:	n/a
26	chr3:47292165-47292215	GM12892	blood:	n/a
27	chr3:47292165-47292215	U87	brain:	n/a
28	chr3:47292165-47292215	HepG2	liver:	n/a
29	chr3:47292165-47292215	Hela-S3	cervix:	n/a
30	chr3:47292165-47292215	NHDF-neo	bronchial:	n/a
31	chr3:47292165-47292215	NH-A	brain:	n/a
32	chr3:47292165-47292215	HCF	heart:	n/a
33	chr3:47292165-47292215	H1-hESC	embryonic stem cell:	embryo
34	chr3:47292165-47292215	Caco-2	colon:	n/a
35	chr3:47292165-47292215	PFSK-1	brain:	n/a
36	chr3:47292165-47292215	SK-N-SH	brain:	n/a
37	chr3:47292165-47292215	HNPCEpiC	eye:	n/a
38	chr3:47292165-47292215	HCT-116	colon:	n/a
39	chr3:47292165-47292215	NB4	blood:	n/a
40	chr3:47292165-47292215	MCF-7	breast:	n/a
41	chr3:47292165-47292215	AG04450	lung:	fetal
42	chr3:47292165-47292215	PANC-1	pancreas:	n/a
43	chr3:47292165-47292215	GM19239	blood:	n/a
44	chr3:47292165-47292215	RPTEC	kidney:	n/a
45	chr3:47292165-47292215	HIPEpiC	eye:	n/a
46	chr3:47292165-47292215	A549	lung:	n/a
47	chr3:47292165-47292215	LNCaP	prostate:	n/a
48	chr3:47292165-47292215	K562	blood:	n/a
49	chr3:47292165-47292215	PrEC	prostate:	n/a
50	chr3:47292165-47292215	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:47290764..47292267-chr3:47322907..47324747,2	K562	blood:
2	chr3:47291529..47292509-chr8:33370744..33371736,2	MCF-7	breast:
3	chr3:47292029..47293531-chr8:33370667..33372185,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000239128	TF binding region
ENSG00000239128	CpG island
ENSG00000088727	Chromatin interaction
ENSG00000239039	Chromatin interaction
ENSG00000129696	Chromatin interaction
ENSG00000114648	Chromatin interaction

Extended variants
information (count: 82 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs1038394	0.96[CEU][hapmap];0.81[JPT][hapmap];0.91[TSI][hapmap]
rs1076394	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10865946	0.96[CEU][hapmap]
rs11130115	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.98[TSI][hapmap]
rs11130123	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11130126	0.92[CEU][hapmap];0.93[TSI][hapmap];0.90[EUR][1000 genomes]
rs11130128	0.96[CEU][hapmap];0.81[JPT][hapmap]
rs11130129	0.96[CEU][hapmap];0.82[JPT][hapmap]
rs11705957	0.96[CEU][hapmap];0.81[JPT][hapmap];0.91[TSI][hapmap]
rs11710013	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11710121	0.85[CEU][hapmap]
rs11710322	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11711824	0.96[CEU][hapmap];0.81[JPT][hapmap];0.91[TSI][hapmap]
rs11712445	0.96[CEU][hapmap]
rs11714294	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11719877	0.96[CEU][hapmap];0.93[TSI][hapmap]
rs11915074	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs11920354	0.81[EUR][1000 genomes]
rs11920853	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs11921117	0.90[EUR][1000 genomes]
rs12636851	0.96[CEU][hapmap];0.81[JPT][hapmap];0.89[TSI][hapmap]
rs13061071	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.95[JPT][hapmap];0.98[TSI][hapmap]
rs13072802	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13075233	0.96[CEU][hapmap];0.93[TSI][hapmap]
rs13094438	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1531875	0.96[CEU][hapmap];0.81[JPT][hapmap];0.93[TSI][hapmap]
rs1638676	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17080872	0.81[JPT][hapmap]
rs17410853	0.85[CEU][hapmap]
rs17411375	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap]
rs17476234	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1872164	0.96[CEU][hapmap];0.81[JPT][hapmap];0.91[TSI][hapmap]
rs2088135	0.82[EUR][1000 genomes]
rs2132173	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.95[TSI][hapmap];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2159400	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];0.95[JPT][hapmap];0.93[TSI][hapmap]
rs2276853	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2276854	0.94[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[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs295428	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap]
rs295441	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs295442	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.80[MKK][hapmap];0.98[TSI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs295449	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.98[TSI][hapmap]
rs295458	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap]
rs295461	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];0.95[JPT][hapmap];0.98[TSI][hapmap]
rs3736177	0.96[CEU][hapmap]
rs4078466	0.89[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];0.95[LWK][hapmap];0.96[MKK][hapmap];0.95[TSI][hapmap];0.96[YRI][hapmap]
rs4082155	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];0.95[TSI][hapmap]
rs4682852	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap]
rs4683322	0.81[CEU][hapmap];0.89[TSI][hapmap]
rs4683324	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4683326	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858811	0.96[CEU][hapmap];0.81[JPT][hapmap]
rs4858824	0.96[CEU][hapmap]
rs4858868	0.96[CEU][hapmap];0.93[TSI][hapmap]
rs4858893	0.96[CEU][hapmap];0.85[JPT][hapmap]
rs4858894	0.87[CEU][hapmap];0.88[JPT][hapmap]
rs56250009	0.82[EUR][1000 genomes]
rs58472056	0.80[EUR][1000 genomes]
rs59689369	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62248905	0.80[EUR][1000 genomes]
rs6767907	0.81[CEU][hapmap];0.91[TSI][hapmap]
rs6768221	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs6772670	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]
rs6780013	0.89[CEU][hapmap];0.84[TSI][hapmap]
rs6791842	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.93[LWK][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6792461	0.96[CEU][hapmap];0.81[JPT][hapmap];0.89[TSI][hapmap]
rs6800271	0.96[CEU][hapmap];0.81[JPT][hapmap];0.91[TSI][hapmap]
rs7632501	0.82[EUR][1000 genomes]
rs7636423	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7651762	0.96[CEU][hapmap];0.81[JPT][hapmap]
rs807932	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs807935	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs807936	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs807937	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs811115	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs922957	0.96[CEU][hapmap]
rs9311403	0.84[CEU][hapmap]
rs9683033	0.96[CEU][hapmap];0.81[JPT][hapmap];0.89[TSI][hapmap]
rs9837343	0.81[CEU][hapmap];0.91[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876756	chr3:47002931-47586514	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
2	nsv1007714	chr3:47084387-47331570	Transcr. at gene 5' and 3' Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	nsv1014457	chr3:47222292-47335175	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv536560	chr3:47222292-47335175	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs11130124	KLHL18	Cis_1M	lymphoblastoid	RTeQTL
rs11130124	SETD2	Cis_1M	lymphoblastoid	RTeQTL
rs11130124	CCHCR1	trans	lymphoblastoid	seeQTL

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47264200-47322200	Weak transcription	Gastric	stomach
2	chr3:47267200-47308000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr3:47270800-47307800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:47271400-47308000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr3:47276400-47305200	Weak transcription	Brain Anterior Caudate	brain
6	chr3:47277600-47300400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:47282200-47300400	Weak transcription	Fetal Intestine Small	intestine
8	chr3:47282200-47300600	Weak transcription	Lung	lung
9	chr3:47282600-47292400	Weak transcription	Fetal Muscle Trunk	muscle
10	chr3:47282800-47322400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr3:47283400-47293200	Weak transcription	Psoas Muscle	Psoas
12	chr3:47284800-47300400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:47285400-47315800	Weak transcription	Pancreas	Pancrea
14	chr3:47285600-47312400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr3:47286400-47299200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr3:47287200-47293200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr3:47287400-47299200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr3:47291000-47293000	Enhancers	Liver	Liver
19	chr3:47291800-47292400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr3:47291800-47292600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr3:47291800-47292600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:47291800-47293600	Enhancers	HepG2	liver
23	chr3:47292000-47292400	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr3:47292000-47292600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr3:47292000-47292600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr3:47292000-47292600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr3:47292000-47292800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:47292000-47293400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr3:47292000-47293400	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr3:47292000-47293600	Enhancers	K562	blood

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