Variant report

Variant	rs10158935
Chromosome Location	chr1:155631546-155631547
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:155619365..155621539-chr1:155630413..155632008,2	K562	blood:
2	chr1:155629015..155630662-chr1:155630856..155633669,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000246203	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs13374779	0.85[AFR][1000 genomes]
rs13375894	0.97[AFR][1000 genomes]
rs16836971	0.97[AFR][1000 genomes]
rs57208252	0.85[AFR][1000 genomes]
rs58774418	1.00[AFR][1000 genomes]
rs59287240	0.97[AFR][1000 genomes]
rs7550827	0.95[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529709	chr1:155154933-155757219	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
2	esv33869	chr1:155223283-155917961	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
3	esv3431739	chr1:155514331-155664183	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer 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	61 gene(s)	inside rSNPs	diseases
4	esv3388968	chr1:155532335-155658278	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
5	nsv1002390	chr1:155553423-155706930	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv428246	chr1:155558197-155785831	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
7	nsv436522	chr1:155559513-155674249	Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
8	esv3360339	chr1:155562157-155683127	Active TSS Flanking Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
9	nsv547965	chr1:155563152-155688600	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats 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	41 gene(s)	inside rSNPs	diseases
10	esv3381327	chr1:155582853-155718436	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	esv3436971	chr1:155618172-155733386	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
12	esv3338099	chr1:155618190-155733359	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155617800-155637000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:155618800-155631800	Weak transcription	K562	blood
3	chr1:155625600-155635400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:155626600-155641800	Weak transcription	Fetal Heart	heart
5	chr1:155627000-155641000	Strong transcription	Fetal Stomach	stomach
6	chr1:155627000-155657600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr1:155627200-155636800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:155627200-155639600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:155627200-155640800	Strong transcription	Thymus	Thymus
10	chr1:155627200-155641000	Strong transcription	Fetal Muscle Leg	muscle
11	chr1:155627200-155648200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr1:155627200-155651600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:155627200-155654000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:155627400-155634600	Strong transcription	Primary B cells from cord blood	blood
15	chr1:155627400-155635800	Weak transcription	Fetal Kidney	kidney
16	chr1:155627600-155632400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:155627600-155650200	Strong transcription	GM12878-XiMat	blood
18	chr1:155627600-155650600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:155627600-155653600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:155627800-155650600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:155628000-155632200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr1:155628000-155632800	Strong transcription	HSMM	muscle
23	chr1:155628000-155633000	Strong transcription	Esophagus	oesophagus
24	chr1:155628000-155639400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:155628000-155641000	Strong transcription	Fetal Muscle Trunk	muscle
26	chr1:155628000-155641200	Strong transcription	Fetal Intestine Small	intestine
27	chr1:155628000-155641400	Strong transcription	Liver	Liver
28	chr1:155628000-155647600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:155628000-155648000	Strong transcription	Primary hematopoietic stem cells	blood
30	chr1:155628000-155650400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:155628000-155650400	Strong transcription	Duodenum Smooth Muscle	Duodenum
32	chr1:155628000-155650400	Strong transcription	Stomach Smooth Muscle	stomach
33	chr1:155628000-155650600	Strong transcription	HUES6 Cell Line	embryonic stem cell
34	chr1:155628000-155650600	Strong transcription	Primary B cells from peripheral blood	blood
35	chr1:155628000-155650600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr1:155628000-155650600	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr1:155628000-155650800	Strong transcription	Primary T cells from cord blood	blood
38	chr1:155628000-155650800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:155628000-155650800	Strong transcription	Placenta	Placenta
40	chr1:155628000-155651600	Strong transcription	Adipose Nuclei	Adipose
41	chr1:155628000-155652000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr1:155628000-155652000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:155628000-155653800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr1:155628000-155654600	Strong transcription	Fetal Thymus	thymus
45	chr1:155628200-155632600	Strong transcription	HSMMtube	muscle
46	chr1:155628200-155634400	Strong transcription	Fetal Brain Female	brain
47	chr1:155628200-155634600	Strong transcription	A549	lung
48	chr1:155628200-155636800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr1:155628200-155641000	Strong transcription	Ovary	ovary
50	chr1:155628200-155641400	Strong transcription	Lung	lung

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