Variant report

Variant	rs4620533
Chromosome Location	chr1:155262613-155262614
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:155261117..155264004-chr1:155277463..155281311,3	MCF-7	breast:
2	chr1:155261455..155264148-chr1:155268677..155271659,2	MCF-7	breast:
3	chr1:155256966..155259263-chr1:155261793..155263472,2	MCF-7	breast:
4	chr1:155245531..155248491-chr1:155261533..155265348,4	MCF-7	breast:
5	chr1:155220670..155222238-chr1:155260191..155263130,2	MCF-7	breast:
6	chr1:155261026..155263305-chr1:155270752..155272531,2	K562	blood:
7	chr1:155260049..155265292-chr1:155266559..155270522,5	K562	blood:

Variant related genes	Relation type
ENSG00000176444	Chromatin interaction
ENSG00000160767	Chromatin interaction
ENSG00000143627	Chromatin interaction
ENSG00000160752	Chromatin interaction
ENSG00000143630	Chromatin interaction

Extended variants
information (count: 126 )
Associated
traits (count: 21 )

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs10128085	0.82[EUR][1000 genomes]
rs1045253	0.81[ASN][1000 genomes]
rs1046188	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1052176	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1052177	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1076556	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1078699	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10796940	0.81[ASN][1000 genomes]
rs10796941	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10796943	0.82[CHB][hapmap];0.90[TSI][hapmap]
rs10796945	0.84[CHB][hapmap];0.85[TSI][hapmap]
rs10908459	0.82[ASN][1000 genomes]
rs10908461	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10908462	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10908463	0.96[CEU][hapmap];0.84[CHB][hapmap];0.86[MEX][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10908465	0.84[CEU][hapmap];0.84[CHB][hapmap];0.85[TSI][hapmap]
rs11264343	0.81[ASN][1000 genomes]
rs11264345	0.82[ASN][1000 genomes]
rs11264346	0.94[ASN][1000 genomes]
rs11264347	0.83[EUR][1000 genomes]
rs11264348	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11264349	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11264351	0.90[ASN][1000 genomes]
rs11264352	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11264353	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11264354	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11264355	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11264357	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11264358	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11264359	0.81[ASW][hapmap];0.92[CEU][hapmap];0.90[CHB][hapmap];0.83[CHD][hapmap];0.87[GIH][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11264361	0.96[CEU][hapmap];0.84[CHB][hapmap];0.80[CHD][hapmap];0.86[MEX][hapmap];0.97[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11264367	0.84[CEU][hapmap];0.84[CHB][hapmap]
rs11264369	0.84[CHB][hapmap]
rs11264371	0.84[CHB][hapmap]
rs11264372	0.84[CHB][hapmap]
rs11264375	0.84[CEU][hapmap];0.84[CHB][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap]
rs1142287	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11577338	0.95[ASN][1000 genomes]
rs12026638	0.89[CHB][hapmap];0.85[TSI][hapmap]
rs12032720	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12034326	0.83[ASN][1000 genomes]
rs12041534	0.84[CEU][hapmap];0.84[CHB][hapmap];0.81[MEX][hapmap];0.85[TSI][hapmap]
rs12042020	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12044063	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12049375	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12067675	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12239114	0.84[CEU][hapmap];0.84[CHB][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap]
rs12407919	0.81[ASN][1000 genomes]
rs12563994	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12723761	0.80[ASN][1000 genomes]
rs12724079	0.84[CHB][hapmap]
rs12724449	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12732972	0.82[ASN][1000 genomes]
rs12748155	0.86[ASN][1000 genomes]
rs12749306	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1325908	0.84[CHB][hapmap]
rs1546818	0.89[ASN][1000 genomes]
rs1800438	0.82[ASN][1000 genomes]
rs1807042	0.85[ASN][1000 genomes]
rs1886905	0.80[CEU][hapmap]
rs2009578	0.82[ASN][1000 genomes]
rs2071053	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2072647	0.88[ASN][1000 genomes]
rs2075566	0.93[ASN][1000 genomes]
rs2075569	0.82[ASN][1000 genomes]
rs2236863	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2236864	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2242576	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2242577	0.93[ASN][1000 genomes]
rs2297480	0.96[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.97[TSI][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2361536	0.88[ASN][1000 genomes]
rs2361543	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3020781	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34906309	0.89[ASN][1000 genomes]
rs3754485	0.82[ASN][1000 genomes]
rs3762272	0.92[ASN][1000 genomes]
rs3768566	0.81[ASN][1000 genomes]
rs3814318	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3814319	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4043	0.81[ASN][1000 genomes]
rs4971072	0.83[ASN][1000 genomes]
rs5005770	0.84[CEU][hapmap];0.84[CHB][hapmap];0.85[TSI][hapmap]
rs56310840	0.81[ASN][1000 genomes]
rs59062514	0.86[ASN][1000 genomes]
rs6672284	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs734073	0.89[ASN][1000 genomes]
rs734074	0.88[ASN][1000 genomes]
rs741756	0.86[ASN][1000 genomes]
rs7520184	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7524950	0.99[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7534795	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7543234	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7549276	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7554780	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs762488	0.82[ASN][1000 genomes]
rs8177968	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8847	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs932972	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9426886	0.83[JPT][hapmap]
rs9628662	0.82[ASN][1000 genomes]
rs9729564	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532579	chr1:154548165-155262692	Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	575 gene(s)	inside rSNPs	diseases
2	nsv831614	chr1:155094978-155275031	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	434 gene(s)	inside rSNPs	diseases
3	esv2757756	chr1:155094978-155314807	Bivalent Enhancer Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	452 gene(s)	inside rSNPs	diseases
4	esv2758971	chr1:155094978-155314807	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	452 gene(s)	inside rSNPs	diseases
5	nsv872457	chr1:155135335-155310443	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	407 gene(s)	inside rSNPs	diseases
6	nsv831625	chr1:155145634-155313409	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	407 gene(s)	inside rSNPs	diseases
7	nsv529709	chr1:155154933-155757219	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
8	esv1832331	chr1:155213136-155271366	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
9	esv1826485	chr1:155214478-155264270	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
10	nsv831636	chr1:155219223-155444864	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
11	esv33869	chr1:155223283-155917961	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
12	esv17013	chr1:155227059-155262674	Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
13	esv1797617	chr1:155228592-155264270	Genic enhancers Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
14	esv1829849	chr1:155228592-155264270	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
15	esv1826924	chr1:155230444-155271566	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
16	esv1830821	chr1:155230610-155265661	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
17	esv1831955	chr1:155230610-155265661	Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
18	esv1826761	chr1:155230622-155262613	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription 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	31 gene(s)	inside rSNPs	diseases
19	esv1826280	chr1:155230622-155262851	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
20	esv1832100	chr1:155230622-155269896	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
21	esv1827811	chr1:155230644-155271366	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
22	esv1827924	chr1:155230644-155271366	Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
23	esv1831963	chr1:155239116-155267459	Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
24	esv1830532	chr1:155239128-155267471	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
25	nsv872466	chr1:155259025-155269991	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:21)

SNP	Gene	Cis/trans	Tissue	Source
rs4620533	SPRR2A	cis	cerebellum	SCAN
rs4620533	THBS3	cis	Whole Blood	GTEx
rs4620533	PKLR	cis	Nerve Tibial	GTEx
rs4620533	GBA	cis	Esophagus Mucosa	GTEx
rs4620533	GBAP1	cis	Thyroid	GTEx
rs4620533	LAMTOR2	cis	lymphoblastoid	seeQTL
rs4620533	RP11-263K19.4	cis	Whole Blood	GTEx
rs4620533	FDPS	Cis_1M	lymphoblastoid	RTeQTL
rs4620533	HCN3	cis	multi-tissue	Pritchard
rs4620533	GBAP1	cis	Artery Tibial	GTEx
rs4620533	YY1AP1	cis	cerebellum	SCAN
rs4620533	FDPS	cis	parietal	SCAN
rs4620533	LCE1C	cis	parietal	SCAN
rs4620533	RIT1	Cis_1M	lymphoblastoid	RTeQTL
rs4620533	THEM5	cis	parietal	SCAN
rs4620533	ADAM15	cis	multi-tissue	Pritchard
rs4620533	DCST1	cis	parietal	SCAN
rs4620533	GBAP1	cis	parietal	SCAN
rs4620533	FDPS	cis	lymphoblastoid	seeQTL
rs4620533	CRNN	cis	cerebellum	SCAN
rs4620533	SCNM1	cis	parietal	SCAN

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155248200-155262800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:155248800-155264800	Weak transcription	Pancreas	Pancrea
3	chr1:155249000-155262800	Weak transcription	Colonic Mucosa	Colon
4	chr1:155249400-155263200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr1:155249400-155264800	Weak transcription	Brain Angular Gyrus	brain
6	chr1:155253000-155262800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr1:155253800-155263000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr1:155254600-155263200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr1:155254600-155264400	Weak transcription	Spleen	Spleen
10	chr1:155255200-155263200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr1:155255400-155263000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr1:155257000-155262800	Strong transcription	Fetal Intestine Small	intestine
13	chr1:155258200-155263000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:155258400-155264600	Weak transcription	Esophagus	oesophagus
15	chr1:155258600-155264400	Weak transcription	Gastric	stomach
16	chr1:155258800-155262800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr1:155258800-155263200	Weak transcription	Fetal Intestine Large	intestine
18	chr1:155259000-155263000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:155259000-155264000	Strong transcription	Liver	Liver
20	chr1:155261200-155264800	Strong transcription	K562	blood
21	chr1:155262600-155262800	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:155262600-155263200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:155262600-155264400	Strong transcription	HepG2	liver

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