Variant report

Variant	rs73240832
Chromosome Location	chr14:34801649-34801650
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:34800554..34803623-chr14:34808126..34810131,3	K562	blood:
2	chr14:34799600..34803505-chr14:35015683..35020657,6	K562	blood:
3	chr14:34799049..34803588-chr14:34929796..34932817,6	MCF-7	breast:
4	chr14:34801106..34802609-chr14:34842166..34844322,2	MCF-7	breast:
5	chr14:34799548..34803609-chr14:34964477..34969425,6	MCF-7	breast:
6	chr14:34799146..34802383-chr14:35022565..35025550,6	K562	blood:
7	chr14:34801000..34803505-chr14:35018421..35020509,2	K562	blood:
8	chr14:34800539..34802093-chr14:34803618..34805977,2	K562	blood:
9	chr14:34800512..34802884-chr14:34930105..34932182,2	K562	blood:
10	chr14:34800052..34803596-chr14:35017115..35019908,4	MCF-7	breast:
11	chr14:34799658..34804397-chr14:34825720..34832179,6	MCF-7	breast:
12	chr14:34800025..34801871-chr14:35015919..35018818,2	MCF-7	breast:
13	chr14:34796387..34803256-chr14:34929329..34933926,13	MCF-7	breast:
14	chr14:34800941..34803201-chr14:34806783..34809053,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000165389	Chromatin interaction
ENSG00000129521	Chromatin interaction
ENSG00000206596	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10129413	0.96[EUR][1000 genomes]
rs10136010	1.00[EUR][1000 genomes]
rs10146683	0.86[EUR][1000 genomes]
rs10747292	0.96[EUR][1000 genomes]
rs11156838	0.96[EUR][1000 genomes]
rs12435087	0.96[EUR][1000 genomes]
rs1958573	0.96[EUR][1000 genomes]
rs1958574	0.96[EUR][1000 genomes]
rs1958575	0.96[EUR][1000 genomes]
rs1958576	0.96[EUR][1000 genomes]
rs1958577	0.96[EUR][1000 genomes]
rs4246986	0.96[EUR][1000 genomes]
rs4981229	0.93[EUR][1000 genomes]
rs4982165	0.96[EUR][1000 genomes]
rs6571649	0.96[EUR][1000 genomes]
rs7149091	0.83[EUR][1000 genomes]
rs7149706	0.96[EUR][1000 genomes]
rs73240826	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8009491	0.96[EUR][1000 genomes]
rs8022686	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 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	esv34180	chr14:34480514-34838295	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	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
8	esv2754221	chr14:34783048-34838295	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv901599	chr14:34792079-34828738	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	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

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:34800600-34802000	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr14:34800600-34802000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:34800600-34802000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr14:34800800-34802200	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr14:34800800-34802400	Enhancers	Liver	Liver
6	chr14:34801000-34801800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr14:34801000-34801800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr14:34801000-34801800	Enhancers	Stomach Mucosa	stomach
9	chr14:34801000-34802000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:34801000-34802000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr14:34801000-34802000	Enhancers	Fetal Muscle Leg	muscle
12	chr14:34801000-34802000	Flanking Active TSS	A549	lung
13	chr14:34801000-34802000	Flanking Active TSS	Hela-S3	cervix
14	chr14:34801000-34802000	Flanking Bivalent TSS/Enh	HepG2	liver
15	chr14:34801000-34802000	Enhancers	K562	blood
16	chr14:34801000-34802200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr14:34801000-34802200	Flanking Active TSS	GM12878-XiMat	blood
18	chr14:34801000-34802400	Enhancers	Fetal Muscle Trunk	muscle
19	chr14:34801000-34802400	Enhancers	Placenta	Placenta
20	chr14:34801200-34802000	Enhancers	H1 Cell Line	embryonic stem cell
21	chr14:34801200-34802000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr14:34801200-34802000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr14:34801200-34802000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:34801200-34802000	Enhancers	Duodenum Mucosa	Duodenum
25	chr14:34801200-34802000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr14:34801200-34802000	Enhancers	Osteobl	bone
27	chr14:34801200-34802200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr14:34801200-34802200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr14:34801200-34802200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr14:34801200-34802200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr14:34801400-34801800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr14:34801400-34801800	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr14:34801400-34802000	Enhancers	NH-A	brain
34	chr14:34801400-34802200	Enhancers	Esophagus	oesophagus
35	chr14:34801600-34802200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
36	chr14:34801600-34802200	Enhancers	Small Intestine	intestine
37	chr14:34801600-34802200	Enhancers	NHEK	skin
38	chr14:34801600-34803200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr14:34801600-34803400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr14:34801600-34804600	Weak transcription	Primary B cells from peripheral blood	blood
41	chr14:34801600-34805400	Weak transcription	Fetal Intestine Large	intestine

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