Variant report

Variant	rs11737590
Chromosome Location	chr4:151751369-151751370
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:151744686..151747422-chr4:151749185..151751868,3	K562	blood:

Extended variants
information (count: 131 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:106)

rs_ID	r²[population]
rs10003857	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10012460	0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10025414	1.00[CEU][hapmap];0.89[GIH][hapmap];0.82[TSI][hapmap];0.84[YRI][hapmap]
rs10222881	0.91[TSI][hapmap]
rs10520078	0.86[GIH][hapmap]
rs10857250	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1148631	0.82[EUR][1000 genomes]
rs1148633	0.82[EUR][1000 genomes]
rs1148634	0.82[EUR][1000 genomes]
rs1148636	0.82[EUR][1000 genomes]
rs1148641	0.82[EUR][1000 genomes]
rs1148644	0.82[EUR][1000 genomes]
rs1148646	0.82[EUR][1000 genomes]
rs1148650	0.81[EUR][1000 genomes]
rs1148651	0.84[EUR][1000 genomes]
rs1148655	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1201197	0.82[EUR][1000 genomes]
rs1201199	0.82[EUR][1000 genomes]
rs1201200	0.82[EUR][1000 genomes]
rs1201204	0.98[ASN][1000 genomes]
rs1201208	0.80[GIH][hapmap];0.91[TSI][hapmap];0.82[EUR][1000 genomes]
rs1201209	0.82[EUR][1000 genomes]
rs1201210	0.91[TSI][hapmap];0.82[EUR][1000 genomes]
rs1201216	0.84[EUR][1000 genomes]
rs1212119	0.80[EUR][1000 genomes]
rs12499833	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12508892	0.89[GIH][hapmap];0.82[TSI][hapmap]
rs12645871	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12648430	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1273331	0.82[EUR][1000 genomes]
rs1273332	0.82[EUR][1000 genomes]
rs1298678	0.82[EUR][1000 genomes]
rs13126388	0.81[EUR][1000 genomes]
rs1451634	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1583188	0.82[EUR][1000 genomes]
rs1583189	0.82[EUR][1000 genomes]
rs17027030	1.00[CEU][hapmap]
rs17027034	1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[LWK][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs17027100	0.80[AFR][1000 genomes]
rs17027155	0.90[EUR][1000 genomes]
rs17027197	0.82[EUR][1000 genomes]
rs1782360	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1782365	0.82[EUR][1000 genomes]
rs184150	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs186080	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1947314	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2154349	0.82[EUR][1000 genomes]
rs2198191	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2198192	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2218899	0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs294530	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs294531	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs294532	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];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs294533	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs294535	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4318628	0.89[GIH][hapmap]
rs4336207	0.80[GIH][hapmap]
rs4355367	1.00[CEU][hapmap];0.89[GIH][hapmap];0.82[TSI][hapmap]
rs4416458	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4533751	1.00[CEU][hapmap];0.89[GIH][hapmap];0.82[TSI][hapmap]
rs4696220	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4696222	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4696630	0.84[ASN][1000 genomes]
rs4696632	0.89[EUR][1000 genomes]
rs4696634	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4696648	0.91[TSI][hapmap]
rs57003564	0.90[EUR][1000 genomes]
rs62344569	0.83[AFR][1000 genomes]
rs62344602	0.82[EUR][1000 genomes]
rs62346265	0.80[AFR][1000 genomes]
rs62346301	0.83[AFR][1000 genomes]
rs62346303	0.81[AFR][1000 genomes]
rs62346304	0.82[AFR][1000 genomes]
rs62346308	0.80[AFR][1000 genomes]
rs62346309	0.80[AFR][1000 genomes]
rs62346311	0.83[AFR][1000 genomes]
rs62346341	0.82[AFR][1000 genomes]
rs62346345	0.80[AFR][1000 genomes]
rs62346349	0.95[AFR][1000 genomes]
rs62346350	0.84[AFR][1000 genomes]
rs62346351	0.88[AFR][1000 genomes]
rs6535749	0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6535750	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6811016	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6817726	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6820819	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6831200	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6836017	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6838286	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6841158	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6851019	0.88[ASN][1000 genomes]
rs6852035	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6854740	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6855472	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73859222	0.80[AFR][1000 genomes]
rs7655761	0.84[ASN][1000 genomes]
rs7656796	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7663641	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7671635	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7677186	0.80[AFR][1000 genomes]
rs7677374	0.80[GIH][hapmap];0.91[TSI][hapmap];0.82[EUR][1000 genomes]
rs7682370	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7698142	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs891689	0.80[GIH][hapmap];0.91[TSI][hapmap];0.82[EUR][1000 genomes]
rs971640	1.00[CEU][hapmap]
rs9884181	0.80[GIH][hapmap]

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	nsv880256	chr4:151126725-151751369	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv817540	chr4:151228965-151858609	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1024820	chr4:151364078-151943561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv1032070	chr4:151514664-151775259	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1034948	chr4:151590115-152202687	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
6	nsv537302	chr4:151590115-152202687	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	nsv530159	chr4:151624865-152203910	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	nsv1018404	chr4:151664438-152067409	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv1017850	chr4:151664438-152071876	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
10	esv2763837	chr4:151664438-152071888	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
11	nsv870257	chr4:151665349-152072867	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
12	nsv1015387	chr4:151673751-152071876	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
13	nsv526976	chr4:151675819-152055073	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
14	nsv1025077	chr4:151682266-152035733	Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Weak 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
15	nsv537303	chr4:151682266-152035733	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS 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
16	nsv949066	chr4:151693149-152069566	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
17	nsv949002	chr4:151693149-152095109	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
18	nsv948719	chr4:151693149-152161625	Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
19	nsv1031720	chr4:151708502-152071876	Strong transcription Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
20	nsv880262	chr4:151712054-152519899	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
21	nsv1031516	chr4:151718614-152065644	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
22	nsv537304	chr4:151718614-152065644	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
23	nsv1022884	chr4:151718814-152065505	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
24	nsv537305	chr4:151718814-152065505	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
25	nsv880576	chr4:151751369-151936149	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151713000-151761200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr4:151724400-151770600	Weak transcription	A549	lung
3	chr4:151724800-151763400	Weak transcription	Esophagus	oesophagus
4	chr4:151726600-151780400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr4:151735000-151773000	Weak transcription	Hela-S3	cervix
6	chr4:151737200-151754000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:151737200-151775000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr4:151737400-151772800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:151738400-151770400	Weak transcription	Brain Substantia Nigra	brain
10	chr4:151738400-151775200	Weak transcription	Osteobl	bone
11	chr4:151740000-151773600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr4:151743000-151761200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:151743800-151772800	Weak transcription	Placenta	Placenta
14	chr4:151743800-151795600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:151744000-151761200	Weak transcription	Psoas Muscle	Psoas
16	chr4:151744200-151751800	Weak transcription	Fetal Heart	heart
17	chr4:151744200-151753000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr4:151745000-151780600	Weak transcription	Colon Smooth Muscle	Colon
19	chr4:151745600-151752000	Strong transcription	Primary T cells from cord blood	blood
20	chr4:151746200-151751800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr4:151746200-151764200	Weak transcription	Lung	lung
22	chr4:151746400-151775000	Weak transcription	HSMM	muscle
23	chr4:151746800-151770000	Weak transcription	NHEK	skin
24	chr4:151747800-151752200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr4:151748000-151752400	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr4:151748200-151752000	Weak transcription	Stomach Mucosa	stomach
27	chr4:151748200-151752600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr4:151748200-151756000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr4:151748400-151774600	Weak transcription	Small Intestine	intestine
30	chr4:151748400-151795600	Weak transcription	Brain Angular Gyrus	brain
31	chr4:151749400-151775200	Weak transcription	NH-A	brain
32	chr4:151749600-151761200	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr4:151749600-151770400	Weak transcription	HUVEC	blood vessel
34	chr4:151749600-151770600	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr4:151749600-151772400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr4:151749800-151752400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:151749800-151752400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:151749800-151754200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr4:151749800-151759400	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr4:151749800-151759400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:151749800-151759400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:151749800-151759400	Weak transcription	Primary hematopoietic stem cells	blood
43	chr4:151749800-151759800	Weak transcription	Fetal Lung	lung
44	chr4:151749800-151760400	Weak transcription	Adipose Nuclei	Adipose
45	chr4:151749800-151760400	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr4:151749800-151761000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr4:151749800-151761000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr4:151749800-151761000	Weak transcription	Ovary	ovary
49	chr4:151749800-151761000	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr4:151749800-151761000	Weak transcription	Rectal Mucosa Donor 31	rectum

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