Variant report

Variant	rs28621834
Chromosome Location	chr15:55975254-55975255
allele	C/T
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	EP300	chr15:55975196-55976586	SK-N-SH	brain:	n/a	chr15:55976401-55976411
2	STAT3	chr15:55975061-55975260	MCF10A-Er-Src	breast:	n/a	chr15:55975228-55975236

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:55973838..55975695-chr15:56033955..56035878,2	MCF-7	breast:

Variant related genes	Relation type
PRTG	TF binding region
ENSG00000166450	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16976467	0.90[AFR][1000 genomes]
rs28428526	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28481986	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28557162	0.81[AFR][1000 genomes]
rs28576513	0.80[AFR][1000 genomes]
rs28620386	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62017991	1.00[EUR][1000 genomes]
rs6493806	0.80[AFR][1000 genomes]
rs7162504	0.81[AFR][1000 genomes]
rs7164032	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7179697	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8027291	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8032175	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917323	chr15:55290499-56041334	Genic enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv1043789	chr15:55400872-56092454	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv948522	chr15:55639867-56032099	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent Enhancer 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 miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv457157	chr15:55722213-56255774	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv569539	chr15:55722213-56255774	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
6	nsv1049774	chr15:55759573-56044600	Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
7	nsv457158	chr15:55930542-55982257	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv569541	chr15:55930542-55982257	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv833017	chr15:55965957-56157912	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55911800-55977000	Weak transcription	Fetal Intestine Small	intestine
2	chr15:55920800-55987600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:55932600-55987000	Weak transcription	Ovary	ovary
4	chr15:55954000-55975400	Weak transcription	HSMM	muscle
5	chr15:55954000-55977400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr15:55954400-55987000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr15:55955400-55980000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr15:55958200-55977600	Weak transcription	Fetal Muscle Trunk	muscle
9	chr15:55958800-55977400	Weak transcription	Left Ventricle	heart
10	chr15:55960400-55977600	Weak transcription	Placenta	Placenta
11	chr15:55960800-55995800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr15:55963400-55980200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:55964000-55977200	Weak transcription	HUVEC	blood vessel
14	chr15:55964200-55975600	Weak transcription	Fetal Stomach	stomach
15	chr15:55964800-55977200	Weak transcription	HepG2	liver
16	chr15:55969000-55975600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr15:55969000-55976000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr15:55969000-55976800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr15:55969000-55987000	Weak transcription	Fetal Lung	lung
20	chr15:55969200-55975600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr15:55969200-55980200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr15:55969200-55986000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr15:55969400-55980200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr15:55970400-55977800	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr15:55970600-55976800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:55970800-55977400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr15:55971200-55976200	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr15:55972000-55986400	Weak transcription	Fetal Intestine Large	intestine
29	chr15:55973600-55975400	Weak transcription	Right Atrium	heart
30	chr15:55973800-55976000	Strong transcription	Fetal Kidney	kidney
31	chr15:55974200-55976000	Strong transcription	Hela-S3	cervix
32	chr15:55974200-55976800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr15:55974200-55978600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr15:55974400-55976000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr15:55974400-55976200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr15:55974600-55976000	Weak transcription	GM12878-XiMat	blood
37	chr15:55974600-55977800	Weak transcription	Primary hematopoietic stem cells	blood
38	chr15:55975000-55976200	Strong transcription	A549	lung
39	chr15:55975200-55976200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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