Variant report

Variant	rs4845635
Chromosome Location	chr1:154474131-154474132
allele	C/G
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	E2F6	chr1:154474013-154475849	H1-hESC	embryonic stem cell:	n/a	chr1:154475683-154475692 chr1:154474738-154474747 chr1:154475247-154475254 chr1:154474983-154474992 chr1:154475362-154475374 chr1:154475038-154475048
2	CEBPB	chr1:154474069-154474504	H1-hESC	embryonic stem cell:	n/a	chr1:154474300-154474311
3	MAX	chr1:154474033-154475830	H1-hESC	embryonic stem cell:	n/a	chr1:154474736-154474746 chr1:154475552-154475562 chr1:154474854-154474864 chr1:154475484-154475493 chr1:154474576-154474585 chr1:154475160-154475179 chr1:154475164-154475175
4	POLR2A	chr1:154473932-154474266	HUVEC	blood vessel:	n/a	n/a
5	CEBPB	chr1:154474120-154474489	IMR90	lung:	n/a	chr1:154474300-154474311
6	MAX	chr1:154474027-154475856	H1-hESC	embryonic stem cell:	n/a	chr1:154474736-154474746 chr1:154475552-154475562 chr1:154474854-154474864 chr1:154475484-154475493 chr1:154474576-154474585 chr1:154475160-154475179 chr1:154475164-154475175
7	CEBPB	chr1:154474117-154474492	HepG2	liver:	n/a	chr1:154474300-154474311
8	CEBPB	chr1:154473971-154474633	A549	lung:	n/a	chr1:154474300-154474311
9	CEBPB	chr1:154474047-154474519	MCF-7	breast:	n/a	chr1:154474300-154474311
10	SUZ12	chr1:154473918-154474502	H1-hESC	embryonic stem cell:	n/a	n/a
11	GABPA	chr1:154474068-154474427	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr1:154474113-154474492	HepG2	liver:	n/a	chr1:154474300-154474311
13	POLR2A	chr1:154474018-154475497	HUVEC	blood vessel:	n/a	n/a
14	CEBPB	chr1:154474124-154474479	ECC-1	luminal epithelium:	n/a	chr1:154474300-154474311
15	YY1	chr1:154474119-154474525	H1-hESC	embryonic stem cell:	n/a	n/a
16	ZBTB7A	chr1:154474065-154474588	ECC-1	luminal epithelium:	n/a	n/a
17	E2F6	chr1:154473973-154475840	H1-hESC	embryonic stem cell:	n/a	chr1:154475683-154475692 chr1:154474738-154474747 chr1:154475247-154475254 chr1:154474983-154474992 chr1:154475362-154475374 chr1:154475038-154475048
18	POLR2A	chr1:154473755-154475537	HUVEC	blood vessel:	n/a	n/a
19	CEBPB	chr1:154474119-154474493	K562	blood:	n/a	chr1:154474300-154474311
20	CEBPB	chr1:154474046-154474595	ECC-1	luminal epithelium:	n/a	chr1:154474300-154474311

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:154474108-154474158	GM12878	blood:	n/a
2	chr1:154474108-154474158	PrEC	prostate:	n/a
3	chr1:154474108-154474158	HepG2	liver:	n/a
4	chr1:154474108-154474158	IMR90	lung:	fetal
5	chr1:154474108-154474158	HCT-116	colon:	n/a
6	chr1:154474108-154474158	ProgFib	skin:	n/a
7	chr1:154474108-154474158	SK-N-SH_RA	brain:	n/a
8	chr1:154474108-154474158	HCF	heart:	n/a
9	chr1:154474108-154474158	MCF-7	breast:	n/a
10	chr1:154474108-154474158	SK-N-MC	brain:	n/a
11	chr1:154474108-154474158	HCM	heart:	n/a
12	chr1:154474108-154474158	HEK293	kidney:	embryo
13	chr1:154474108-154474158	GM12892	blood:	n/a
14	chr1:154474108-154474158	ECC-1	luminal epithelium:	n/a
15	chr1:154474108-154474158	HEEpiC	esophagus:	n/a
16	chr1:154474108-154474158	RPTEC	kidney:	n/a
17	chr1:154474108-154474158	CMK	blood:	n/a
18	chr1:154474108-154474158	NHBE	bronchial:	n/a
19	chr1:154474108-154474158	BJ	skin:	n/a
20	chr1:154474108-154474158	PANC-1	pancreas:	n/a
21	chr1:154474108-154474158	AG04449	skin:	fetal
22	chr1:154474108-154474158	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:154474108-154474158	SK-N-SH	brain:	n/a
24	chr1:154474108-154474158	AG09309	skin:	n/a
25	chr1:154474108-154474158	AG09319	gingival:	n/a
26	chr1:154474108-154474158	HRPEpiC	eye:	n/a
27	chr1:154474108-154474158	BE2_C	brain:	n/a
28	chr1:154474108-154474158	AG10803	skin:	n/a
29	chr1:154474108-154474158	H1-hESC	embryonic stem cell:	embryo
30	chr1:154474108-154474158	Hela-S3	cervix:	n/a
31	chr1:154474108-154474158	NH-A	brain:	n/a
32	chr1:154474108-154474158	AoSMC	blood vessel:	n/a
33	chr1:154474108-154474158	T-47D	breast:	n/a
34	chr1:154474108-154474158	NB4	blood:	n/a
35	chr1:154474108-154474158	HMEC	breast:	n/a
36	chr1:154474108-154474158	A549	lung:	n/a
37	chr1:154474108-154474158	ovcar-3	ovarian:	n/a
38	chr1:154474108-154474158	HL-60	blood:	n/a
39	chr1:154474108-154474158	HNPCEpiC	eye:	n/a
40	chr1:154474108-154474158	LNCaP	prostate:	n/a
41	chr1:154474108-154474158	HIPEpiC	eye:	n/a
42	chr1:154474108-154474158	MCF10A-Er-Src	breast:	n/a
43	chr1:154474108-154474158	NT2-D1	testis:	n/a
44	chr1:154474108-154474158	HUVEC	blood vessel:	n/a
45	chr1:154474108-154474158	HRCEpiC	kidney:	n/a
46	chr1:154474108-154474158	NHDF-neo	bronchial:	n/a
47	chr1:154474108-154474158	SAEC	small airway:	n/a
48	chr1:154474108-154474158	Jurkat	blood:	n/a
49	chr1:154474108-154474158	Hepatocyte	liver:	n/a
50	chr1:154474108-154474158	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:154473384..154476326-chr1:154529885..154532539,2	MCF-7	breast:
2	chr1:154191216..154193063-chr1:154472171..154474701,2	K562	blood:

Variant related genes	Relation type
TDRD10	TF binding region
TDRD10	CpG island
ENSG00000143569	Chromatin interaction
ENSG00000160714	Chromatin interaction
ENSG00000143612	Chromatin interaction

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10159236	0.87[EUR][1000 genomes]
rs10752642	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10752643	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10908844	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10908846	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11265627	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11265629	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11265634	0.91[EUR][1000 genomes]
rs11804305	0.85[EUR][1000 genomes]
rs12118074	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12124333	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12129484	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs14021	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16836054	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41302545	0.95[EUR][1000 genomes]
rs4131514	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4269769	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4288587	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4307559	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4307560	0.86[AFR][1000 genomes]
rs4308966	0.87[EUR][1000 genomes]
rs4329505	0.87[EUR][1000 genomes]
rs4345796	0.86[EUR][1000 genomes]
rs4393148	0.82[YRI][hapmap]
rs4474240	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4518898	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4575077	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4585969	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4845632	0.82[YRI][hapmap]
rs4845634	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4845636	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4845640	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4845641	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4845643	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4845644	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4845648	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56047170	0.89[EUR][1000 genomes]
rs56233546	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61811362	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61812599	0.84[EUR][1000 genomes]
rs61812626	0.86[EUR][1000 genomes]
rs61812631	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61812654	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6427716	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6427720	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6427721	0.86[AFR][1000 genomes]
rs6427722	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6427724	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6656395	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6662503	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6670375	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6683078	0.82[YRI][hapmap]
rs6687112	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6689710	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6691727	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6696177	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6697103	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6697115	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6701586	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6703672	0.91[EUR][1000 genomes]
rs72698167	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7513603	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7526247	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7539745	0.96[EUR][1000 genomes]
rs7543174	0.88[EUR][1000 genomes]
rs7550664	0.94[EUR][1000 genomes]
rs7553602	0.93[EUR][1000 genomes]
rs9427076	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9427082	0.95[EUR][1000 genomes]
rs9427415	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv948413	chr1:153974621-154797272	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
2	nsv1000402	chr1:153991106-154527053	Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases
3	nsv521887	chr1:154236570-154684106	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
4	esv1815481	chr1:154465065-154475033	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	esv3424713	chr1:154473153-154475701	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	esv3414034	chr1:154473478-154476776	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv547942	chr1:154474131-154474784	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	nsv547943	chr1:154474131-154474875	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv547944	chr1:154474131-154474977	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv547945	chr1:154474131-154475033	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	nsv547946	chr1:154474131-154475037	Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
12	esv1822921	chr1:154474131-154495697	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:154471200-154475400	Active TSS	Right Atrium	heart
2	chr1:154471800-154474200	Bivalent/Poised TSS	Psoas Muscle	Psoas
3	chr1:154472000-154475200	Bivalent/Poised TSS	Left Ventricle	heart
4	chr1:154472200-154475400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
5	chr1:154472200-154475400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
6	chr1:154472400-154474400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
7	chr1:154472400-154475400	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
8	chr1:154472600-154474200	Bivalent/Poised TSS	Fetal Lung	lung
9	chr1:154472800-154474800	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
10	chr1:154472800-154475200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:154472800-154475200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
12	chr1:154472800-154475200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
13	chr1:154473000-154474200	Bivalent/Poised TSS	Fetal Thymus	thymus
14	chr1:154473000-154475000	Active TSS	Lung	lung
15	chr1:154473200-154474400	Flanking Active TSS	Liver	Liver
16	chr1:154473200-154475200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
17	chr1:154473200-154475200	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
18	chr1:154473200-154475600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
19	chr1:154473200-154475600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr1:154473400-154474800	Bivalent/Poised TSS	Aorta	Aorta
21	chr1:154473400-154475000	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
22	chr1:154473400-154475200	Active TSS	HUVEC	blood vessel
23	chr1:154473400-154475400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
24	chr1:154473600-154474200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:154473800-154474200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
26	chr1:154473800-154474200	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
27	chr1:154473800-154474200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
28	chr1:154473800-154474200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
29	chr1:154473800-154474200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
30	chr1:154473800-154474200	Flanking Active TSS	Ovary	ovary
31	chr1:154473800-154474200	Flanking Active TSS	Right Ventricle	heart
32	chr1:154473800-154474200	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
33	chr1:154473800-154474400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:154473800-154474400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:154473800-154474400	Bivalent/Poised TSS	Brain Substantia Nigra	brain
36	chr1:154473800-154474400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
37	chr1:154473800-154474600	Bivalent/Poised TSS	Brain Angular Gyrus	brain
38	chr1:154473800-154474600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
39	chr1:154473800-154474800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
40	chr1:154473800-154474800	Flanking Active TSS	Pancreas	Pancrea
41	chr1:154473800-154475200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
42	chr1:154473800-154475200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
43	chr1:154473800-154475400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
44	chr1:154473800-154475400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
45	chr1:154473800-154475400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
46	chr1:154473800-154475400	Bivalent Enhancer	Primary B cells from cord blood	blood
47	chr1:154473800-154475400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
48	chr1:154473800-154475400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
49	chr1:154473800-154475400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:154473800-154475400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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