Variant report

Variant	rs2938343
Chromosome Location	chr1:114581604-114581605
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:114565136..114566738-chr1:114579035..114581815,2	MCF-7	breast:
2	chr1:114572795..114577655-chr1:114580622..114587867,10	MCF-7	breast:
3	chr1:114577897..114580371-chr1:114581560..114584344,2	MCF-7	breast:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10776776	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10776777	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11102721	0.95[ASN][1000 genomes]
rs11102722	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1394075	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1587773	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1604781	0.93[ASN][1000 genomes]
rs1910486	0.93[ASN][1000 genomes]
rs2938317	0.95[ASN][1000 genomes]
rs2938321	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2938324	0.95[ASN][1000 genomes]
rs2938325	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2938334	0.93[ASN][1000 genomes]
rs2938335	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2938336	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2938337	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2938338	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2938339	0.93[ASN][1000 genomes]
rs2938340	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2938341	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2938342	0.93[ASN][1000 genomes]
rs2938344	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2938345	0.93[ASN][1000 genomes]
rs2938349	0.91[ASN][1000 genomes]
rs2938350	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2938351	0.93[ASN][1000 genomes]
rs3006985	0.84[ASN][1000 genomes]
rs3006986	0.84[ASN][1000 genomes]
rs3006991	0.93[ASN][1000 genomes]
rs3006992	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3006993	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs3006994	0.93[ASN][1000 genomes]
rs3006995	0.93[ASN][1000 genomes]
rs3006997	0.93[ASN][1000 genomes]
rs3007004	0.93[ASN][1000 genomes]
rs3007005	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs3007007	0.93[ASN][1000 genomes]
rs3007010	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752424	chr1:114189958-114712958	Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	esv2754686	chr1:114531958-114602958	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv1849780	chr1:114577463-114663164	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:114576000-114582800	Weak transcription	HSMMtube	muscle
2	chr1:114576000-114583400	Weak transcription	Lung	lung
3	chr1:114576600-114582800	Weak transcription	Fetal Intestine Large	intestine
4	chr1:114577200-114583200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:114577400-114582000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:114577800-114583000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr1:114578000-114582200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:114578200-114583000	Enhancers	H9 Cell Line	embryonic stem cell
9	chr1:114578600-114582400	Enhancers	H1 Cell Line	embryonic stem cell
10	chr1:114579000-114583800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr1:114579400-114582000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:114579600-114581800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:114580200-114581800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:114580200-114582000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr1:114580200-114583000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr1:114580600-114582400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:114580800-114582000	Enhancers	NHEK	skin
18	chr1:114580800-114583800	Enhancers	Fetal Intestine Small	intestine
19	chr1:114581000-114583000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr1:114581200-114582000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr1:114581200-114582200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr1:114581200-114582600	Weak transcription	HMEC	breast
23	chr1:114581200-114582800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr1:114581200-114584800	Weak transcription	Fetal Muscle Leg	muscle
25	chr1:114581400-114581800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr1:114581400-114582200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr1:114581400-114583400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:114581600-114582000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr1:114581600-114582600	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr1:114581600-114585400	Enhancers	Primary monocytes fromperipheralblood	blood

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