Variant report

Variant	rs61171197
Chromosome Location	chr14:34838904-34838905
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:34836857..34839880-chr14:35023528..35025416,3	MCF-7	breast:
2	chr14:34836485..34839521-chr14:34847849..34850157,3	MCF-7	breast:
3	chr14:34830868..34842924-chr14:34928180..34935370,25	MCF-7	breast:
4	chr14:34835401..34839083-chr14:34893653..34895439,3	MCF-7	breast:
5	chr14:34836773..34839966-chr14:34841911..34844333,3	MCF-7	breast:
6	chr14:34838344..34842091-chr14:34845007..34847766,4	MCF-7	breast:
7	chr14:34836399..34839473-chr14:34930536..34933225,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000129521	Chromatin interaction
ENSG00000165389	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11844733	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11848977	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11851994	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11852014	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17102454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17102460	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17102468	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1958587	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1958588	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4982174	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58047097	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74046040	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74046041	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74046042	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs74046043	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][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	nsv1040980	chr14:34345018-35255592	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
2	nsv1051104	chr14:34592378-35007083	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv949738	chr14:34616331-34990688	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv564192	chr14:34725233-34996507	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer 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	13 gene(s)	inside rSNPs	diseases
5	nsv564193	chr14:34728127-35000188	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer 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	13 gene(s)	inside rSNPs	diseases
6	nsv528989	chr14:34744426-34998705	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS 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	13 gene(s)	inside rSNPs	diseases
7	esv2761577	chr14:34792079-34839752	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv1054949	chr14:34834260-34992049	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
9	nsv542025	chr14:34834260-34992049	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:34831400-34839400	Weak transcription	Lung	lung
2	chr14:34831600-34840000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:34835800-34843200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr14:34836400-34839400	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr14:34836600-34839200	Enhancers	Fetal Intestine Small	intestine
6	chr14:34836600-34839400	Enhancers	Stomach Mucosa	stomach
7	chr14:34836800-34840000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr14:34837000-34839200	Enhancers	Fetal Intestine Large	intestine
9	chr14:34837000-34839200	Enhancers	NHEK	skin
10	chr14:34837000-34839400	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr14:34837200-34839000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr14:34837200-34839200	Enhancers	Placenta Amnion	Placenta Amnion
13	chr14:34837200-34839200	Enhancers	HMEC	breast
14	chr14:34837200-34839800	Enhancers	Placenta	Placenta
15	chr14:34837400-34840400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr14:34837800-34839000	Enhancers	Adipose Nuclei	Adipose
17	chr14:34838000-34839000	Enhancers	Primary B cells from cord blood	blood
18	chr14:34838000-34842200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr14:34838200-34839200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr14:34838400-34839000	Enhancers	Primary hematopoietic stem cells	blood
21	chr14:34838400-34839200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr14:34838400-34839200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr14:34838400-34844000	Weak transcription	Pancreas	Pancrea
24	chr14:34838600-34839200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr14:34838600-34839200	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr14:34838600-34844000	Weak transcription	Colonic Mucosa	Colon
27	chr14:34838800-34839200	Weak transcription	Fetal Lung	lung
28	chr14:34838800-34840200	Enhancers	Hela-S3	cervix
29	chr14:34838800-34841200	Weak transcription	HepG2	liver
30	chr14:34838800-34841800	Weak transcription	A549	lung
31	chr14:34838800-34844000	Weak transcription	Duodenum Mucosa	Duodenum
32	chr14:34838800-34844000	Weak transcription	Rectal Mucosa Donor 29	rectum

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