Variant report

Variant	rs564309
Chromosome Location	chr1:228585562-228585563
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:228578293-228588731	K562	blood:	n/a	n/a
2	POLR2A	chr1:228581121-228585848	K562	blood:	n/a	n/a
3	POLR2A	chr1:228585110-228585861	K562	blood:	n/a	n/a
4	POLR2A	chr1:228584900-228585614	K562	blood:	n/a	n/a
5	POLR2A	chr1:228584938-228585820	GM12892	blood:	n/a	n/a
6	POLR2A	chr1:228584932-228585872	GM12878	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228584060..228585786-chr1:228588820..228591560,2	MCF-7	breast:
2	chr1:228582272..228585110-chr1:228585474..228588026,2	MCF-7	breast:
3	chr1:228581680..228585660-chr1:228593046..228594989,3	MCF-7	breast:
4	chr1:228540204..228544343-chr1:228583648..228586877,3	K562	blood:
5	chr1:228585219..228604537-chr1:228641966..228650471,45	MCF-7	breast:

No data

Variant related genes	Relation type
TRIM11	TF binding region
ENSG00000154370	Chromatin interaction
ENSG00000181218	Chromatin interaction
ENSG00000154358	Chromatin interaction
ENSG00000196890	Chromatin interaction
ENSG00000266174	Chromatin interaction

Extended variants
information (count: 114 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs1007686	0.84[GIH][hapmap]
rs10157289	0.91[EUR][1000 genomes]
rs10158088	0.81[EUR][1000 genomes]
rs10158354	0.91[EUR][1000 genomes]
rs10158680	0.91[EUR][1000 genomes]
rs10916313	0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10916317	0.84[GIH][hapmap]
rs1150917	0.94[ASN][1000 genomes]
rs1150918	0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11555960	0.89[EUR][1000 genomes]
rs11581974	0.90[CHB][hapmap];0.89[GIH][hapmap];0.94[JPT][hapmap];0.83[TSI][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11587839	0.88[ASN][1000 genomes]
rs1188473	0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1188474	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1188482	0.95[CHB][hapmap];0.89[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1188483	0.95[CHB][hapmap];0.89[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1188485	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1188487	0.95[CHB][hapmap];0.89[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1188488	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1188489	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12027720	0.88[EUR][1000 genomes]
rs12031395	0.91[EUR][1000 genomes]
rs12061320	0.85[CHB][hapmap]
rs12061490	0.85[CEU][hapmap];0.90[CHB][hapmap];0.89[CHD][hapmap];0.88[JPT][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs12061642	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12061733	0.83[EUR][1000 genomes]
rs12065660	0.85[CEU][hapmap];0.91[EUR][1000 genomes]
rs12065815	0.91[EUR][1000 genomes]
rs12081278	0.83[JPT][hapmap]
rs12082349	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12085738	0.85[CEU][hapmap];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12089997	0.91[EUR][1000 genomes]
rs12093491	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12094956	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12096217	0.85[CEU][hapmap];0.82[TSI][hapmap];0.84[EUR][1000 genomes]
rs12691493	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12725863	0.88[ASN][1000 genomes]
rs12735877	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12751024	1.00[CEU][hapmap];1.00[MEX][hapmap];0.82[TSI][hapmap];0.84[EUR][1000 genomes]
rs12760907	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13373984	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2230656	0.95[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34090141	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34673199	0.91[EUR][1000 genomes]
rs35155240	0.91[EUR][1000 genomes]
rs35670307	0.84[EUR][1000 genomes]
rs35711644	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3738687	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3795785	0.88[JPT][hapmap]
rs3795790	0.81[CHB][hapmap]
rs3795800	0.86[CHB][hapmap];0.83[JPT][hapmap]
rs3795810	0.85[CEU][hapmap];0.86[CHB][hapmap];0.81[CHD][hapmap];0.83[JPT][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs3795811	0.90[CHB][hapmap];0.89[CHD][hapmap];0.88[JPT][hapmap]
rs3795814	0.85[CEU][hapmap];0.86[CHB][hapmap];0.81[CHD][hapmap];0.83[JPT][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs4065231	0.90[EUR][1000 genomes]
rs4581279	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4653551	0.95[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs4653552	0.87[ASN][1000 genomes]
rs4653960	0.83[ASN][1000 genomes]
rs474600	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs491670	0.86[EUR][1000 genomes]
rs493950	0.95[GIH][hapmap];0.88[EUR][1000 genomes]
rs493954	0.89[EUR][1000 genomes]
rs494154	0.87[CHB][hapmap];0.89[EUR][1000 genomes]
rs503203	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs503391	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs505129	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs513467	0.83[CHB][hapmap];1.00[GIH][hapmap];0.89[EUR][1000 genomes]
rs532465	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs538604	0.88[EUR][1000 genomes]
rs538851	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs541959	0.91[EUR][1000 genomes]
rs56174824	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs572442	0.93[EUR][1000 genomes]
rs573128	0.82[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs58462432	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61825312	0.91[EUR][1000 genomes]
rs61825336	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61825338	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61827276	0.83[EUR][1000 genomes]
rs6426501	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6426503	0.84[GIH][hapmap]
rs6659690	0.88[ASN][1000 genomes]
rs6666241	0.88[ASN][1000 genomes]
rs7513530	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7524236	0.95[CHB][hapmap];0.89[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7529055	0.84[GIH][hapmap]
rs7555386	0.88[ASN][1000 genomes]
rs9787095	0.91[EUR][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	esv32853	chr1:227880116-228806209	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
2	nsv826908	chr1:227895386-228691100	Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
3	nsv523935	chr1:228038124-228681749	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
4	nsv873255	chr1:228254753-228684779	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS 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	133 gene(s)	inside rSNPs	diseases
5	nsv827019	chr1:228314167-228651020	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases
6	nsv873267	chr1:228434395-228585837	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
7	nsv873270	chr1:228442663-228699477	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
8	nsv1009891	chr1:228450763-228742676	Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
9	nsv873274	chr1:228450868-228585837	Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
10	nsv873275	chr1:228456147-228585837	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
11	nsv517545	chr1:228456147-228685999	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
12	nsv873276	chr1:228456943-228585837	Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
13	nsv1013500	chr1:228459134-228849601	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
14	nsv873278	chr1:228464248-228585837	Strong transcription Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
15	nsv468271	chr1:228464248-228601638	Bivalent Enhancer Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
16	nsv468283	chr1:228464248-228601638	Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
17	nsv468294	chr1:228464248-228601638	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS 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 miRNA target site	27 gene(s)	inside rSNPs	diseases
18	nsv549295	chr1:228464248-228601638	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
19	nsv470780	chr1:228464248-228606965	Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
20	nsv873279	chr1:228494790-228681195	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
21	nsv873280	chr1:228500627-228603029	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
22	nsv873281	chr1:228505739-228656780	Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
23	esv1808261	chr1:228509427-228674518	Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
24	esv2829948	chr1:228509427-228687948	Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
25	nsv508697	chr1:228540037-228622614	Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Hip circumference (psychosocial stress interaction)	25271088	GWAS catalog

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs564309	RHOU	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228567000-228592800	Weak transcription	Fetal Kidney	kidney
2	chr1:228569800-228585600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:228571000-228591600	Weak transcription	Fetal Brain Male	brain
4	chr1:228577000-228592600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr1:228577400-228590800	Weak transcription	Right Atrium	heart
6	chr1:228579000-228590600	Strong transcription	Gastric	stomach
7	chr1:228579000-228591200	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr1:228579000-228592000	Strong transcription	Fetal Stomach	stomach
9	chr1:228579200-228588400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr1:228579400-228590600	Strong transcription	Duodenum Mucosa	Duodenum
11	chr1:228579400-228590800	Strong transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:228579400-228591800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr1:228579400-228592000	Strong transcription	Fetal Intestine Small	intestine
14	chr1:228579600-228591000	Strong transcription	Liver	Liver
15	chr1:228579600-228591600	Strong transcription	Fetal Brain Female	brain
16	chr1:228579600-228591600	Strong transcription	Thymus	Thymus
17	chr1:228579600-228592000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr1:228579800-228588600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:228579800-228590800	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr1:228579800-228591800	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr1:228579800-228591800	Strong transcription	Brain Germinal Matrix	brain
22	chr1:228579800-228591800	Strong transcription	Fetal Thymus	thymus
23	chr1:228579800-228592600	Strong transcription	HUES48 Cell Line	embryonic stem cell
24	chr1:228580000-228585600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr1:228580000-228591200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:228580000-228591800	Strong transcription	Cortex derived primary cultured neurospheres	brain
27	chr1:228580000-228592000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:228580200-228591800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr1:228580800-228590600	Strong transcription	Primary B cells from peripheral blood	blood
30	chr1:228581000-228586000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:228581000-228586000	Strong transcription	GM12878-XiMat	blood
32	chr1:228581000-228592400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr1:228581200-228592800	Weak transcription	Psoas Muscle	Psoas
34	chr1:228581400-228585800	Strong transcription	Brain Anterior Caudate	brain
35	chr1:228581400-228589400	Strong transcription	Dnd41	blood
36	chr1:228581600-228586400	Strong transcription	Primary B cells from cord blood	blood
37	chr1:228581600-228591200	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr1:228581600-228591200	Strong transcription	Stomach Smooth Muscle	stomach
39	chr1:228581600-228592000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:228581600-228592000	Strong transcription	A549	lung
41	chr1:228581800-228586400	Strong transcription	Placenta Amnion	Placenta Amnion
42	chr1:228581800-228587200	Strong transcription	Brain Cingulate Gyrus	brain
43	chr1:228581800-228590000	Strong transcription	Esophagus	oesophagus
44	chr1:228581800-228590000	Strong transcription	NHEK	skin
45	chr1:228581800-228591200	Strong transcription	Fetal Intestine Large	intestine
46	chr1:228582000-228586000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:228582000-228586000	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr1:228582000-228587000	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr1:228582000-228589200	Strong transcription	Pancreas	Pancrea
50	chr1:228582000-228590200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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