Variant report

Variant	rs3759903
Chromosome Location	chr15:99768642-99768643
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	chr15:99761212..99763784-chr15:99766463..99769175,2	MCF-7	breast:
2	chr15:99767475..99769524-chr15:99789564..99792407,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000103852	Chromatin interaction
ENSG00000168904	Chromatin interaction

Extended variants
information (count: 109 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10902542	0.81[ASN][1000 genomes]
rs11247069	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11247070	1.00[ASW][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];0.87[LWK][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11247071	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11247076	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs11247077	0.91[CEU][hapmap];1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs11247078	0.91[CEU][hapmap];1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs12439693	0.84[CHB][hapmap]
rs12439819	0.83[CHB][hapmap];0.81[TSI][hapmap]
rs12439820	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12440477	0.89[CHB][hapmap]
rs12440640	0.94[CHB][hapmap]
rs12440737	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12440982	0.89[CHB][hapmap]
rs12441447	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12441965	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs12441996	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12442235	0.89[CHB][hapmap];0.81[TSI][hapmap]
rs12442505	0.91[CEU][hapmap];0.90[CHB][hapmap]
rs12591268	0.91[CEU][hapmap]
rs12591894	0.86[ASN][1000 genomes]
rs12591897	0.81[ASN][1000 genomes]
rs12591991	0.91[CEU][hapmap];0.80[MKK][hapmap];0.86[TSI][hapmap]
rs12592035	0.82[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12592064	0.82[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12592097	1.00[CEU][hapmap];0.93[CHB][hapmap];0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs12593076	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12593192	0.86[ASN][1000 genomes]
rs12593456	0.81[ASN][1000 genomes]
rs12594123	0.91[CEU][hapmap];0.90[CHB][hapmap]
rs12594250	0.91[CEU][hapmap];1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs12594607	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap];0.93[TSI][hapmap];0.81[ASN][1000 genomes]
rs12594709	1.00[CEU][hapmap];0.94[CHB][hapmap]
rs12594851	0.94[AFR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12595099	0.91[CEU][hapmap];0.94[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12595545	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12901547	0.91[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12902590	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12904240	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12906323	0.88[CEU][hapmap];0.94[CHB][hapmap]
rs12906924	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12907938	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12914149	0.82[AFR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12914665	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12917176	0.91[CEU][hapmap]
rs1510058	0.91[CEU][hapmap];0.95[CHB][hapmap];0.83[CHD][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap]
rs1670229	0.82[CHB][hapmap]
rs1876741	0.89[CHB][hapmap]
rs2006670	0.89[CHB][hapmap]
rs2048303	0.90[CEU][hapmap];0.94[CHB][hapmap]
rs2048304	0.91[CEU][hapmap];0.94[CHB][hapmap]
rs2089708	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2136629	1.00[ASW][hapmap];0.91[CEU][hapmap];0.95[CHB][hapmap];0.83[CHD][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap];0.93[TSI][hapmap]
rs2290352	0.83[CHB][hapmap];0.81[TSI][hapmap]
rs2861371	0.94[CHB][hapmap]
rs2862141	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34087342	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34139963	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34258129	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34423043	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34569062	0.81[ASN][1000 genomes]
rs34583616	0.81[ASN][1000 genomes]
rs35103557	0.82[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs35137571	0.94[AFR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35405100	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35703983	0.81[ASN][1000 genomes]
rs35714966	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs36074799	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3784602	0.90[CEU][hapmap];0.94[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3961782	0.90[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4360910	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4965216	0.83[CHB][hapmap]
rs4965446	0.83[CHB][hapmap]
rs4965451	0.89[CHB][hapmap];0.81[TSI][hapmap]
rs71399865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs71403440	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs71403442	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7163435	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7169355	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7170952	1.00[CHB][hapmap];0.95[CHD][hapmap];0.87[GIH][hapmap];0.84[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.83[AMR][1000 genomes]
rs7171061	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7172501	0.89[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7176859	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7177149	0.91[CEU][hapmap];0.84[MKK][hapmap];0.93[TSI][hapmap]
rs7178606	1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];0.84[JPT][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs72756886	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs72756889	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8029457	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8029885	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8031904	0.91[CEU][hapmap];0.94[CHB][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8033266	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531079	chr15:98907913-99878547	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv1039575	chr15:98982045-99924685	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	nsv869529	chr15:99416774-99903351	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv1055008	chr15:99477144-100019861	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1045124	chr15:99504843-99847210	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv904543	chr15:99513231-99991506	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
7	nsv533926	chr15:99519820-99997114	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv915926	chr15:99519820-100138705	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS 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 target site	55 gene(s)	inside rSNPs	diseases
9	nsv1051782	chr15:99621061-99792967	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
10	nsv916822	chr15:99621061-99878564	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
11	nsv949203	chr15:99621061-99932797	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
12	nsv817289	chr15:99621061-100138705	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
13	nsv431411	chr15:99621061-100143999	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
14	nsv570716	chr15:99629901-99916332	Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv904546	chr15:99696046-100166300	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
16	nsv1052528	chr15:99736977-99874210	Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
17	nsv1036346	chr15:99752391-100365458	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
18	nsv542520	chr15:99752391-100365458	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription 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 target site	47 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	chr15:99673200-99789400	Weak transcription	Small Intestine	intestine
2	chr15:99724400-99769600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:99733400-99787400	Weak transcription	NHEK	skin
4	chr15:99749800-99789400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr15:99750000-99789400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr15:99754400-99768800	Strong transcription	Fetal Intestine Large	intestine
7	chr15:99754800-99769000	Strong transcription	Adipose Nuclei	Adipose
8	chr15:99755400-99768800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr15:99756600-99768800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:99756600-99769000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr15:99756600-99789400	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr15:99756800-99768800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr15:99756800-99768800	Strong transcription	Fetal Muscle Trunk	muscle
14	chr15:99756800-99769000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr15:99757600-99768800	Strong transcription	Duodenum Smooth Muscle	Duodenum
16	chr15:99757800-99768800	Strong transcription	Cortex derived primary cultured neurospheres	brain
17	chr15:99757800-99769000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:99758000-99768800	Strong transcription	Stomach Smooth Muscle	stomach
19	chr15:99758200-99769000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr15:99758600-99789400	Weak transcription	Brain Substantia Nigra	brain
21	chr15:99759200-99769800	Weak transcription	Brain Anterior Caudate	brain
22	chr15:99759200-99788400	Weak transcription	Fetal Thymus	thymus
23	chr15:99759400-99769200	Weak transcription	Primary T cells from cord blood	blood
24	chr15:99759400-99781800	Weak transcription	Spleen	Spleen
25	chr15:99759400-99788600	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr15:99759400-99788600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr15:99761000-99778400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr15:99761400-99771000	Weak transcription	GM12878-XiMat	blood
29	chr15:99761400-99781800	Weak transcription	Pancreas	Pancrea
30	chr15:99761400-99788400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr15:99761800-99769800	Weak transcription	Thymus	Thymus
32	chr15:99761800-99772800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr15:99762000-99768800	Strong transcription	Rectal Smooth Muscle	rectum
34	chr15:99762000-99780400	Weak transcription	Esophagus	oesophagus
35	chr15:99762400-99772800	Weak transcription	A549	lung
36	chr15:99762600-99789400	Weak transcription	Gastric	stomach
37	chr15:99762800-99774800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr15:99763200-99768800	Strong transcription	Left Ventricle	heart
39	chr15:99763200-99769000	Strong transcription	HSMMtube	muscle
40	chr15:99763400-99768800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr15:99763800-99769200	Strong transcription	HSMM	muscle
42	chr15:99765000-99769000	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr15:99765000-99769000	Strong transcription	Osteobl	bone
44	chr15:99765200-99768800	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr15:99765200-99769000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr15:99765400-99784000	Weak transcription	Hela-S3	cervix
47	chr15:99765600-99789400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:99765800-99769000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr15:99765800-99769800	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr15:99765800-99778600	Weak transcription	Psoas Muscle	Psoas

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