Variant report

Variant	rs7522928
Chromosome Location	chr1:180491201-180491202
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	TCF7L2	chr1:180490654-180491556	HEK293	kidney:	n/a	chr1:180491376-180491390 chr1:180490862-180490876
2	POLR2A	chr1:180489708-180492117	MCF10A-Er-Src	breast:	n/a	n/a
3	FOS	chr1:180490664-180491947	MCF10A-Er-Src	breast:	n/a	n/a
4	STAT3	chr1:180490620-180492058	MCF10A-Er-Src	breast:	n/a	chr1:180491461-180491481 chr1:180491467-180491475
5	CEBPB	chr1:180490629-180491818	Hela-S3	cervix:	n/a	chr1:180491245-180491256 chr1:180491245-180491258 chr1:180491245-180491256 chr1:180491245-180491258
6	GTF2F1	chr1:180490692-180491606	Hela-S3	cervix:	n/a	n/a
7	FOS	chr1:180490693-180491869	MCF10A-Er-Src	breast:	n/a	n/a
8	CEBPB	chr1:180490643-180491660	HepG2	liver:	n/a	chr1:180491245-180491256 chr1:180491245-180491258 chr1:180491245-180491256 chr1:180491245-180491258
9	FOS	chr1:180490628-180492057	MCF10A-Er-Src	breast:	n/a	n/a
10	TBP	chr1:180490718-180491567	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:180490499-180491275	HCT-116	colon:	n/a	chr1:180491245-180491256 chr1:180491245-180491258 chr1:180491245-180491256 chr1:180491245-180491258
12	SETDB1	chr1:180491166-180491750	U2OS	brain:	n/a	n/a
13	MAX	chr1:180490502-180491386	HCT-116	colon:	n/a	n/a
14	MYC	chr1:180490667-180491990	MCF10A-Er-Src	breast:	n/a	n/a
15	TCF7L2	chr1:180490603-180491456	HCT-116	colon:	n/a	chr1:180491376-180491390 chr1:180490862-180490876
16	FOXA2	chr1:180491148-180491604	HepG2	liver:	n/a	n/a
17	TCF7L2	chr1:180490657-180491371	Hela-S3	cervix:	n/a	chr1:180490862-180490876
18	POLR2A	chr1:180490663-180491601	HepG2	liver:	n/a	n/a
19	TCF7L2	chr1:180490675-180491586	MCF-7	breast:	n/a	chr1:180491376-180491390 chr1:180490862-180490876
20	POLR2A	chr1:180489712-180492297	MCF10A-Er-Src	breast:	n/a	n/a
21	SP1	chr1:180490488-180491209	HCT-116	colon:	n/a	n/a
22	STAT3	chr1:180490715-180491757	MCF10A-Er-Src	breast:	n/a	chr1:180491461-180491481 chr1:180491467-180491475
23	RAD21	chr1:180491083-180491285	HepG2	liver:	n/a	n/a
24	MYC	chr1:180490643-180491502	K562	blood:	n/a	n/a
25	MYC	chr1:180490627-180492029	MCF10A-Er-Src	breast:	n/a	n/a
26	CREB1	chr1:180491197-180491724	HepG2	liver:	n/a	n/a
27	STAT3	chr1:180490631-180492130	MCF10A-Er-Src	breast:	n/a	chr1:180491461-180491481 chr1:180491467-180491475
28	STAT3	chr1:180490601-180492165	MCF10A-Er-Src	breast:	n/a	chr1:180491461-180491481 chr1:180491467-180491475
29	TEAD4	chr1:180491189-180491694	HepG2	liver:	n/a	n/a
30	MAX	chr1:180491075-180491726	HepG2	liver:	n/a	n/a
31	TCF7L2	chr1:180490733-180491382	HepG2	liver:	n/a	chr1:180490862-180490876
32	FOXA1	chr1:180491189-180491568	T-47D	breast:	n/a	n/a
33	FOS	chr1:180490600-180492102	MCF10A-Er-Src	breast:	n/a	n/a
34	TCF7L2	chr1:180490581-180491744	Hela-S3	cervix:	n/a	chr1:180491376-180491390 chr1:180490862-180490876
35	KAP1	chr1:180490647-180491763	U2OS	brain:	n/a	n/a
36	CREB1	chr1:180491200-180491686	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:180472964..180474571-chr1:180490356..180493108,2	MCF-7	breast:
2	chr1:180470877..180472880-chr1:180490627..180493125,2	K562	blood:
3	chr1:180489178..180492158-chr1:180598991..180600573,2	K562	blood:
4	chr1:180490294..180492192-chr1:180552011..180554702,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000206905	TF binding region
ENSG00000135847	Chromatin interaction

Extended variants
information (count: 118 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:115)

rs_ID	r²[population]
rs10157891	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10733004	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes]
rs10733005	0.85[EUR][1000 genomes]
rs10737343	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10737344	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10737345	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10753210	1.00[ASN][1000 genomes]
rs10753213	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10753214	1.00[ASN][1000 genomes]
rs10753217	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10798744	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10798749	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10798763	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10798764	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10913972	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10914011	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10914019	1.00[ASN][1000 genomes]
rs10914020	1.00[ASN][1000 genomes]
rs10914024	0.84[AFR][1000 genomes]
rs1094597	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1094598	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1094599	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12027553	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12077904	1.00[ASN][1000 genomes]
rs12144149	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12565152	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1339722	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1339723	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1339726	1.00[ASN][1000 genomes]
rs1361363	1.00[ASN][1000 genomes]
rs1361628	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1418100	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1418103	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1556935	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1556938	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1591898	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1934411	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1935283	1.00[ASN][1000 genomes]
rs1961741	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2153327	1.00[JPT][hapmap];0.88[EUR][1000 genomes]
rs2153753	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2262371	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2331739	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2331742	0.88[EUR][1000 genomes]
rs2764432	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764434	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764435	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764436	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764437	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764438	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764439	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764440	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764441	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764442	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764444	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2794974	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2794975	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2794976	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4259605	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4281291	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4304539	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4333819	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4532796	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4540612	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4609392	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4651061	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4651063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4651066	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4651067	1.00[ASN][1000 genomes]
rs4652501	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4652502	0.96[EUR][1000 genomes]
rs4652506	1.00[ASN][1000 genomes]
rs4652510	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6425620	1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425621	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425622	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425623	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425624	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425626	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425630	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425642	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425647	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6659147	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6664944	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6665615	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6667478	1.00[ASN][1000 genomes]
rs6669304	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6677367	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6678261	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6680754	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6682067	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs6683484	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6684842	1.00[ASN][1000 genomes]
rs6687873	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6691333	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6695360	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7515052	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7526743	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7529042	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7530015	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[EUR][1000 genomes]
rs7532972	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7542568	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7543143	1.00[ASN][1000 genomes]
rs7546030	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7548707	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7548884	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7555087	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs822704	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs822705	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs863720	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs863721	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9425879	1.00[ASN][1000 genomes]
rs946633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs946634	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs946635	1.00[CEU][hapmap];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762200	chr1:180300936-180493841	ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
2	nsv1003359	chr1:180300936-180727561	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
3	nsv949311	chr1:180438895-180692815	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180486000-180493400	Weak transcription	Fetal Stomach	stomach
2	chr1:180486000-180499400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:180486400-180493800	Weak transcription	Fetal Lung	lung
4	chr1:180488000-180500400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr1:180488200-180492200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr1:180488600-180497000	Enhancers	Placenta	Placenta
7	chr1:180488800-180491800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:180489400-180494400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:180489800-180494400	Weak transcription	HUVEC	blood vessel
10	chr1:180490400-180492000	Enhancers	Placenta Amnion	Placenta Amnion
11	chr1:180490600-180491400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:180490600-180491400	Enhancers	Right Ventricle	heart
13	chr1:180490600-180491400	Enhancers	A549	lung
14	chr1:180490600-180491600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:180490600-180491600	Enhancers	Liver	Liver
16	chr1:180490600-180491600	Enhancers	Psoas Muscle	Psoas
17	chr1:180490600-180491600	Enhancers	Right Atrium	heart
18	chr1:180490600-180491800	Enhancers	Pancreas	Pancrea
19	chr1:180490600-180492000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr1:180490600-180492000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr1:180490600-180492000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr1:180490600-180492400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:180490600-180492600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:180490600-180492800	Enhancers	HMEC	breast
25	chr1:180490800-180491400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:180490800-180491400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:180490800-180491400	Enhancers	Fetal Muscle Leg	muscle
28	chr1:180490800-180491400	Weak transcription	Left Ventricle	heart
29	chr1:180490800-180491600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:180490800-180491600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr1:180490800-180491800	Flanking Active TSS	HepG2	liver
32	chr1:180490800-180492000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr1:180490800-180492000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr1:180490800-180492200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:180490800-180492600	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr1:180490800-180493800	Weak transcription	Lung	lung
37	chr1:180491000-180492000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr1:180491000-180492000	Flanking Active TSS	NHEK	skin
39	chr1:180491000-180499400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr1:180491200-180491400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr1:180491200-180491400	Enhancers	Fetal Heart	heart
42	chr1:180491200-180491400	Flanking Active TSS	Hela-S3	cervix
43	chr1:180491200-180491600	Enhancers	Stomach Mucosa	stomach
44	chr1:180491200-180491600	Flanking Active TSS	HSMMtube	muscle
45	chr1:180491200-180491600	Flanking Active TSS	K562	blood
46	chr1:180491200-180491800	Enhancers	H1 Cell Line	embryonic stem cell
47	chr1:180491200-180491800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr1:180491200-180491800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
49	chr1:180491200-180492000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:180491200-180492000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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