Variant report

Variant	rs10201191
Chromosome Location	chr2:64314603-64314604
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:64309179..64310802-chr2:64312636..64314949,2	MCF-7	breast:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10165165	0.87[ASN][1000 genomes]
rs10169847	0.80[AMR][1000 genomes]
rs10170224	0.84[AMR][1000 genomes]
rs10175483	0.84[AMR][1000 genomes]
rs10183513	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10184867	0.82[ASN][1000 genomes]
rs10191854	0.84[AMR][1000 genomes]
rs10192104	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10192378	0.92[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10204631	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13385515	0.84[AMR][1000 genomes]
rs13400399	0.82[ASN][1000 genomes]
rs13408188	0.84[AMR][1000 genomes]
rs13418461	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13419918	0.80[AMR][1000 genomes]
rs13428357	0.80[AMR][1000 genomes]
rs17028375	0.82[ASN][1000 genomes]
rs28757314	0.87[ASN][1000 genomes]
rs28798530	0.87[ASN][1000 genomes]
rs3731962	0.80[AMR][1000 genomes]
rs3755112	0.80[AMR][1000 genomes]
rs56028117	0.84[AMR][1000 genomes]
rs56301411	0.84[AMR][1000 genomes]
rs7579828	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531376	chr2:64094322-64521876	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv1013132	chr2:64235175-64631084	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats 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	40 gene(s)	inside rSNPs	diseases
3	esv2757803	chr2:64253005-64539556	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	esv2759055	chr2:64253005-64539556	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv428396	chr2:64253005-64539556	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Strong transcription 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	27 gene(s)	inside rSNPs	diseases
6	esv34698	chr2:64312142-64521366	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription 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 target site	26 gene(s)	inside rSNPs	diseases
7	esv34955	chr2:64312182-64521290	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:64302000-64318200	Weak transcription	Fetal Intestine Large	intestine
2	chr2:64303400-64318400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr2:64303800-64318400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr2:64304200-64321600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr2:64305800-64318000	Weak transcription	Fetal Intestine Small	intestine
6	chr2:64307000-64318400	Weak transcription	Placenta	Placenta
7	chr2:64307600-64318400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr2:64309600-64317200	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr2:64309600-64320800	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr2:64311400-64321800	Weak transcription	Small Intestine	intestine
11	chr2:64311800-64316800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr2:64311800-64321200	Weak transcription	K562	blood
13	chr2:64311800-64321800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr2:64311800-64321800	Weak transcription	Brain Germinal Matrix	brain
15	chr2:64312000-64317200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr2:64312200-64318400	Weak transcription	Liver	Liver
17	chr2:64312800-64321200	Weak transcription	Psoas Muscle	Psoas
18	chr2:64313200-64321200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:64313200-64321400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr2:64313200-64321600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:64313200-64321800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr2:64313200-64341800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:64313400-64315400	Weak transcription	HepG2	liver
24	chr2:64313400-64318400	Weak transcription	Adipose Nuclei	Adipose
25	chr2:64313400-64321800	Weak transcription	Brain Angular Gyrus	brain
26	chr2:64313400-64321800	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr2:64313600-64316600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr2:64313600-64317800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr2:64313600-64320600	Weak transcription	Fetal Lung	lung
30	chr2:64313600-64321800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr2:64313600-64323000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr2:64313800-64315400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:64313800-64317000	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr2:64313800-64321800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr2:64313800-64321800	Weak transcription	NH-A	brain
36	chr2:64314200-64318400	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr2:64314200-64321800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr2:64314200-64321800	Weak transcription	Pancreas	Pancrea
39	chr2:64314400-64315600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr2:64314400-64321200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr2:64314400-64325000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr2:64314600-64315400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr2:64314600-64316400	Weak transcription	Primary B cells from peripheral blood	blood
44	chr2:64314600-64316800	Weak transcription	GM12878-XiMat	blood

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