Variant report

Variant	rs7681699
Chromosome Location	chr4:10010520-10010521
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:10009870..10011594-chr4:10018076..10020950,2	MCF-7	breast:
2	chr4:10008851..10011783-chr4:10012924..10016004,5	MCF-7	breast:
3	chr4:10007258..10010277-chr4:10010409..10012241,3	MCF-7	breast:
4	chr4:10008717..10011087-chr4:10117692..10120073,3	MCF-7	breast:
5	chr4:10003454..10005588-chr4:10009688..10011673,2	MCF-7	breast:
6	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000250413	Chromatin interaction
ENSG00000109667	Chromatin interaction
ENSG00000071127	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10939655	0.88[ASN][1000 genomes]
rs10939656	0.88[ASN][1000 genomes]
rs11723970	0.80[ASN][1000 genomes]
rs11732054	0.87[ASN][1000 genomes]
rs11736410	0.88[ASN][1000 genomes]
rs11736479	0.88[ASN][1000 genomes]
rs12499857	0.85[ASN][1000 genomes]
rs12507050	0.90[ASN][1000 genomes]
rs13107466	0.88[ASN][1000 genomes]
rs13113730	0.87[ASN][1000 genomes]
rs13115193	0.80[ASN][1000 genomes]
rs13128214	0.86[ASN][1000 genomes]
rs13133766	0.88[ASN][1000 genomes]
rs17187075	0.86[ASN][1000 genomes]
rs17246501	0.82[ASN][1000 genomes]
rs17246745	0.86[ASN][1000 genomes]
rs17247314	0.90[ASN][1000 genomes]
rs35099040	0.88[ASN][1000 genomes]
rs35438220	0.87[ASN][1000 genomes]
rs35866697	0.88[ASN][1000 genomes]
rs3733586	0.87[ASN][1000 genomes]
rs3756236	0.88[ASN][1000 genomes]
rs3756237	0.88[ASN][1000 genomes]
rs3756238	0.88[ASN][1000 genomes]
rs3796829	0.88[ASN][1000 genomes]
rs3796836	0.88[ASN][1000 genomes]
rs4280729	0.86[ASN][1000 genomes]
rs4622999	0.87[ASN][1000 genomes]
rs6844329	0.86[ASN][1000 genomes]
rs6857693	0.88[ASN][1000 genomes]
rs73227883	0.80[ASN][1000 genomes]
rs7678012	0.86[ASN][1000 genomes]
rs882222	0.80[ASN][1000 genomes]
rs882223	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533218	chr4:9371016-10252290	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	74 gene(s)	inside rSNPs	diseases
2	nsv530090	chr4:9383695-10165033	Enhancers Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
3	nsv1014216	chr4:9713612-10223836	Transcr. at gene 5' and 3' Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
4	nsv1010249	chr4:9716101-10086188	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	nsv878681	chr4:9802853-10397327	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
6	nsv997941	chr4:9805223-10493388	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers 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	54 gene(s)	inside rSNPs	diseases
7	nsv1008649	chr4:9805223-10589802	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
8	nsv1000587	chr4:9805223-10610752	Flanking Active TSS Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
9	nsv537022	chr4:9805223-10610752	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
10	nsv1003454	chr4:9805223-10710990	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
11	nsv537023	chr4:9805223-10710990	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
12	nsv1004801	chr4:9814720-10674528	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
13	nsv537024	chr4:9814720-10674528	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
14	nsv931483	chr4:9814721-10716463	Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
15	esv2763339	chr4:9858426-10056376	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv537026	chr4:9903566-10262258	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
17	nsv1009972	chr4:9903566-10710990	Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
18	nsv537027	chr4:9903566-10710990	Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Genic enhancers 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	58 gene(s)	inside rSNPs	diseases
19	esv2752052	chr4:9911872-10313111	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
20	nsv878688	chr4:9915850-10038112	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	nsv1010620	chr4:9937123-10686682	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
22	nsv530280	chr4:9947818-10940041	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
23	nsv532706	chr4:9948018-10451450	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription 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	50 gene(s)	inside rSNPs	diseases
24	nsv1013022	chr4:9961220-10230042	Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
25	nsv537028	chr4:9961220-10230042	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
26	nsv537029	chr4:9961220-10262258	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
27	nsv878691	chr4:9966477-10418078	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
28	nsv1013487	chr4:9972011-10320963	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
29	nsv829857	chr4:9982514-10155835	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription 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	43 gene(s)	inside rSNPs	diseases
30	nsv469621	chr4:9987670-10142287	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
31	nsv482719	chr4:9987670-10142287	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
32	nsv1008067	chr4:10004664-10262258	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
33	nsv537030	chr4:10004664-10262258	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9998400-10020400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr4:10006800-10012000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:10007000-10012000	Enhancers	Fetal Muscle Leg	muscle
4	chr4:10007200-10011000	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr4:10007200-10011200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:10007200-10012200	Enhancers	Fetal Lung	lung
7	chr4:10007400-10010600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:10007400-10010800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr4:10007400-10010800	Enhancers	Pancreas	Pancrea
10	chr4:10007600-10010600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:10007600-10011600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:10007600-10012800	Enhancers	Fetal Stomach	stomach
13	chr4:10007600-10013200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr4:10007800-10010600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr4:10007800-10011000	Flanking Active TSS	GM12878-XiMat	blood
16	chr4:10008000-10012600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr4:10008200-10011600	Enhancers	Brain Cingulate Gyrus	brain
18	chr4:10008400-10010800	Enhancers	Fetal Thymus	thymus
19	chr4:10008400-10011400	Enhancers	Brain Angular Gyrus	brain
20	chr4:10008600-10011000	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr4:10008600-10011000	Enhancers	Gastric	stomach
22	chr4:10008600-10011600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr4:10008600-10013400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:10008600-10013400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:10008600-10019600	Weak transcription	Right Ventricle	heart
26	chr4:10008600-10020200	Weak transcription	Rectal Smooth Muscle	rectum
27	chr4:10008800-10011600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:10008800-10020200	Weak transcription	Aorta	Aorta
29	chr4:10008800-10020400	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr4:10009000-10011000	Enhancers	Brain Anterior Caudate	brain
31	chr4:10009000-10011000	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr4:10009000-10019800	Weak transcription	Left Ventricle	heart
33	chr4:10009000-10020400	Weak transcription	Lung	lung
34	chr4:10009200-10012200	Enhancers	Brain Hippocampus Middle	brain
35	chr4:10009400-10010800	Enhancers	HSMMtube	muscle
36	chr4:10009400-10011600	Enhancers	NHEK	skin
37	chr4:10009400-10012400	Genic enhancers	HMEC	breast
38	chr4:10009400-10020000	Weak transcription	Colonic Mucosa	Colon
39	chr4:10009600-10013800	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr4:10009600-10015200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:10009800-10010800	Weak transcription	Ovary	ovary
42	chr4:10009800-10019600	Weak transcription	Placenta	Placenta
43	chr4:10010000-10010600	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr4:10010000-10012000	Weak transcription	Fetal Intestine Small	intestine
45	chr4:10010000-10012200	Enhancers	Fetal Heart	heart
46	chr4:10010000-10019800	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr4:10010000-10020200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr4:10010000-10020400	Weak transcription	Esophagus	oesophagus
49	chr4:10010000-10021200	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr4:10010200-10011200	Weak transcription	Small Intestine	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links