Variant report

Variant	rs666569
Chromosome Location	chr1:147010804-147010805
allele	G/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	NR2F2	chr1:147010739-147011420	MCF-7	breast:	n/a	n/a
2	SP1	chr1:147010673-147011449	HCT-116	colon:	n/a	n/a
3	POLR2A	chr1:147010784-147011178	U87	brain:	n/a	n/a
4	CEBPB	chr1:147010799-147011472	IMR90	lung:	n/a	n/a
5	FOS	chr1:147010789-147011351	MCF10A-Er-Src	breast:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011023-147011034 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011051-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011051-147011063
6	SP1	chr1:147010721-147011378	A549	lung:	n/a	n/a
7	POLR2A	chr1:147010778-147011289	HUVEC	blood vessel:	n/a	n/a
8	NFIC	chr1:147010785-147011423	ECC-1	luminal epithelium:	n/a	n/a
9	FOSL2	chr1:147010804-147011239	A549	lung:	n/a	chr1:147011024-147011034 chr1:147011050-147011061 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011035 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011051-147011063
10	FOSL2	chr1:147010728-147011332	MCF-7	breast:	n/a	chr1:147011024-147011034 chr1:147011050-147011061 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011035 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011051-147011063
11	JUND	chr1:147010658-147011367	SK-N-SH	brain:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011023-147011034 chr1:147011051-147011063 chr1:147011051-147011062
12	POLR2A	chr1:147010699-147011294	U87	brain:	n/a	n/a
13	RXRA	chr1:147010696-147011361	SK-N-SH	brain:	n/a	n/a
14	FOSL2	chr1:147010777-147011389	MCF-7	breast:	n/a	chr1:147011024-147011034 chr1:147011050-147011061 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011035 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011051-147011063
15	JUND	chr1:147010720-147011395	SK-N-SH	brain:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011023-147011034 chr1:147011051-147011063 chr1:147011051-147011062
16	MAFK	chr1:147010533-147011336	IMR90	lung:	n/a	n/a
17	EP300	chr1:147010706-147011423	ECC-1	luminal epithelium:	n/a	n/a
18	JUND	chr1:147010762-147011481	HCT-116	colon:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011023-147011034 chr1:147011051-147011063 chr1:147011051-147011062
19	CBX3	chr1:147010742-147011440	HCT-116	colon:	n/a	n/a
20	TCF12	chr1:147010679-147011368	A549	lung:	n/a	n/a
21	TCF12	chr1:147010791-147011484	ECC-1	luminal epithelium:	n/a	n/a
22	SRF	chr1:147010569-147011419	HCT-116	colon:	n/a	n/a
23	JUND	chr1:147010706-147011476	HCT-116	colon:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011023-147011034 chr1:147011051-147011063 chr1:147011051-147011062
24	RCOR1	chr1:147010154-147011747	IMR90	lung:	n/a	n/a
25	ESR1	chr1:147010737-147011283	ECC-1	luminal epithelium:	n/a	n/a
26	STAT3	chr1:147010780-147011068	MCF10A-Er-Src	breast:	n/a	n/a
27	FOSL1	chr1:147010671-147011838	HCT-116	colon:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011034 chr1:147011051-147011062 chr1:147011557-147011565 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011023-147011034 chr1:147011051-147011063
28	FOS	chr1:147010793-147011270	MCF10A-Er-Src	breast:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011023-147011034 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011051-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011051-147011063
29	TCF12	chr1:147010696-147011452	SK-N-SH	brain:	n/a	n/a
30	SRF	chr1:147010712-147011503	HCT-116	colon:	n/a	n/a
31	CEBPB	chr1:147010786-147011365	A549	lung:	n/a	n/a
32	GATA3	chr1:147010645-147011410	A549	lung:	n/a	n/a
33	FOSL1	chr1:147010746-147011429	HCT-116	colon:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011034 chr1:147011051-147011062 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011023-147011034 chr1:147011051-147011063
34	MYC	chr1:147010789-147011263	MCF10A-Er-Src	breast:	n/a	n/a
35	FOSL2	chr1:147010704-147011443	SK-N-SH	brain:	n/a	chr1:147011024-147011034 chr1:147011050-147011061 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011035 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011051-147011063
36	FOS	chr1:147010238-147011326	MCF10A-Er-Src	breast:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011023-147011034 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011051-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011051-147011063
37	FOSL2	chr1:147010692-147011475	A549	lung:	n/a	chr1:147011024-147011034 chr1:147011050-147011061 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011035 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011051-147011063
38	ESR1	chr1:147010736-147011265	ECC-1	luminal epithelium:	n/a	n/a
39	SP1	chr1:147010733-147011357	A549	lung:	n/a	n/a
40	JUN	chr1:147010795-147011424	K562	blood:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011051-147011063
41	SP1	chr1:147010668-147011468	HCT-116	colon:	n/a	n/a
42	NFIC	chr1:147010742-147011513	ECC-1	luminal epithelium:	n/a	n/a
43	KAP1	chr1:147010790-147011353	U2OS	brain:	n/a	chr1:147011026-147011035
44	POLR2A	chr1:147010789-147011200	SK-N-SH	brain:	n/a	n/a
45	CEBPB	chr1:147010692-147011361	HCT-116	colon:	n/a	n/a
46	FOS	chr1:147010762-147011499	MCF10A-Er-Src	breast:	n/a	chr1:147011024-147011034 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011023-147011034 chr1:147011024-147011034 chr1:147011053-147011061 chr1:147011023-147011035 chr1:147011024-147011034 chr1:147011052-147011062 chr1:147011051-147011062 chr1:147011049-147011060 chr1:147011025-147011034 chr1:147011051-147011063

No.	Distal block	Cell Line	Cell type
1	chr1:147009579..147011670-chr1:147058912..147061214,2	MCF-7	breast:
2	chr1:147009715..147011902-chr1:147032676..147034909,2	MCF-7	breast:
3	chr1:147006568..147008358-chr1:147009554..147011067,2	MCF-7	breast:
4	chr1:147010058..147012645-chr11:64784779..64787267,2	MCF-7	breast:
5	chr1:147008733..147014706-chr1:147069097..147075030,9	MCF-7	breast:
6	chr1:147010483..147014086-chr1:147140786..147143809,3	MCF-7	breast:
7	chr1:147004851..147006517-chr1:147008746..147011702,2	MCF-7	breast:
8	chr1:147008618..147011767-chr1:147071183..147073263,3	MCF-7	breast:

Variant related genes	Relation type
BCL9	TF binding region
ENSG00000116128	Chromatin interaction
ENSG00000162836	Chromatin interaction
ENSG00000213465	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10793689	0.84[CHB][hapmap];0.81[JPT][hapmap];0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10900376	0.95[CHB][hapmap];0.89[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.94[MEX][hapmap];0.92[TSI][hapmap];0.92[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12127408	0.85[AMR][1000 genomes]
rs2132440	0.81[JPT][hapmap]
rs3806218	0.95[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.94[MEX][hapmap];0.97[TSI][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4950460	0.85[AMR][1000 genomes]
rs6666306	0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872252	chr1:146471863-147398135	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
2	nsv999546	chr1:146507577-147356574	Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
3	nsv535123	chr1:146507577-147356574	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
4	nsv492188	chr1:146507649-147381479	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
5	nsv916754	chr1:146507711-147417736	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	113 gene(s)	inside rSNPs	diseases
6	nsv547673	chr1:146510112-147398135	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
7	nsv547674	chr1:146522722-147396797	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
8	nsv998341	chr1:146531446-147384720	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
9	nsv535124	chr1:146531446-147384720	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
10	nsv1003493	chr1:146531446-147389944	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
11	nsv998209	chr1:146543722-147384720	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
12	nsv535126	chr1:146543722-147384720	Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
13	nsv872256	chr1:146556596-147410973	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
14	nsv1012331	chr1:146603479-147384720	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
15	nsv535131	chr1:146603479-147384720	Genic enhancers Strong transcription Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
16	nsv1004849	chr1:146661516-147286826	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
17	nsv535135	chr1:146661516-147286826	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
18	nsv534063	chr1:146807433-147381411	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
19	nsv831414	chr1:146884994-147083866	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
20	nsv1001868	chr1:146893791-147389944	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
21	nsv482606	chr1:146959127-147134517	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
22	nsv946307	chr1:146982909-147012496	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs666569	PGAP1	trans	parietal	SCAN
rs666569	FMO5	cis	parietal	SCAN
rs666569	ACP6	cis	parietal	SCAN

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:147006600-147011000	Weak transcription	Left Ventricle	heart
2	chr1:147006600-147012600	Weak transcription	Pancreas	Pancrea
3	chr1:147008400-147012400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr1:147009800-147011200	Enhancers	Ovary	ovary
5	chr1:147009800-147011600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:147009800-147012200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr1:147009800-147012400	Enhancers	Fetal Heart	heart
8	chr1:147010000-147012200	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr1:147010000-147012400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr1:147010000-147012400	Enhancers	NHLF	lung
11	chr1:147010000-147012600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr1:147010000-147012600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:147010000-147012600	Enhancers	Duodenum Mucosa	Duodenum
14	chr1:147010000-147012600	Enhancers	NHDF-Ad	bronchial
15	chr1:147010000-147013200	Enhancers	Hela-S3	cervix
16	chr1:147010200-147011000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr1:147010200-147011000	Enhancers	HSMM	muscle
18	chr1:147010200-147011400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:147010200-147011400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:147010200-147011400	Enhancers	HMEC	breast
21	chr1:147010200-147011800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:147010200-147011800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr1:147010200-147011800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr1:147010200-147011800	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr1:147010200-147011800	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr1:147010200-147011800	Enhancers	A549	lung
27	chr1:147010200-147012000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr1:147010200-147012000	Enhancers	Colon Smooth Muscle	Colon
29	chr1:147010200-147012000	Enhancers	Small Intestine	intestine
30	chr1:147010200-147012200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr1:147010200-147012200	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr1:147010200-147012200	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr1:147010200-147012400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:147010200-147012400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr1:147010200-147012400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:147010200-147012400	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr1:147010200-147012400	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr1:147010200-147012400	Enhancers	Fetal Thymus	thymus
39	chr1:147010200-147012600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:147010200-147012600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:147010200-147012600	Enhancers	Fetal Intestine Large	intestine
42	chr1:147010200-147012600	Enhancers	HSMMtube	muscle
43	chr1:147010200-147012600	Enhancers	NH-A	brain
44	chr1:147010200-147012600	Enhancers	Osteobl	bone
45	chr1:147010400-147011800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr1:147010400-147012200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr1:147010400-147012200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr1:147010400-147012400	Enhancers	Fetal Intestine Small	intestine
49	chr1:147010400-147012400	Enhancers	Fetal Stomach	stomach
50	chr1:147010400-147012400	Enhancers	Rectal Smooth Muscle	rectum

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