Variant report

Variant	rs1204067
Chromosome Location	chr7:104972423-104972424
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	WRNIP1	chr7:104972284-104972455	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:104970954..104972610-chr7:104976907..104979036,2	K562	blood:
2	chr7:104971088..104973665-chr7:105027778..105030280,2	K562	blood:

Variant related genes	Relation type
RNU6-1322P	TF binding region
ENSG00000135250	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10278237	1.00[AMR][1000 genomes]
rs1204057	1.00[AMR][1000 genomes]
rs1204059	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1204063	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1204069	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34588	chr7:104737612-105153242	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	esv2757233	chr7:104758250-105208492	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats 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	39 gene(s)	inside rSNPs	diseases
3	esv2759549	chr7:104758250-105208492	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv8196	chr7:104763559-105155978	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	esv34580	chr7:104763580-105153242	Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription 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 target site	15 gene(s)	inside rSNPs	diseases
6	esv2758127	chr7:104766707-105110581	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv1028228	chr7:104807207-105182998	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
8	nsv932138	chr7:104826194-105152816	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer 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 target site	15 gene(s)	inside rSNPs	diseases
9	nsv1015688	chr7:104849770-105182998	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
10	nsv1029832	chr7:104905057-105112489	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
11	esv2753646	chr7:104905588-104972800	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv1023767	chr7:104931143-105190662	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
13	nsv539049	chr7:104931143-105190662	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
14	nsv1034689	chr7:104950564-105085879	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104945400-104972600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:104948600-104988000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr7:104957400-104986800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:104958000-104983200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr7:104958800-104973000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:104961600-104973000	Weak transcription	Ovary	ovary
7	chr7:104961600-104980200	Weak transcription	Psoas Muscle	Psoas
8	chr7:104961800-104973000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:104962800-104992600	Weak transcription	Fetal Intestine Small	intestine
10	chr7:104963000-104983000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr7:104963200-104991200	Weak transcription	Fetal Stomach	stomach
12	chr7:104963600-104980000	Weak transcription	Brain Anterior Caudate	brain
13	chr7:104964200-104972600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr7:104964200-104977200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr7:104964200-104983200	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr7:104964400-104983400	Weak transcription	Primary T cells from cord blood	blood
17	chr7:104964600-104973000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr7:104966200-104980600	Weak transcription	Primary B cells from cord blood	blood
19	chr7:104966200-104985800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr7:104966800-104973000	Weak transcription	Brain Hippocampus Middle	brain
21	chr7:104967200-104986200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr7:104967800-104973000	Weak transcription	NHEK	skin
23	chr7:104968200-104972600	Weak transcription	Hela-S3	cervix
24	chr7:104968200-104973000	Weak transcription	Pancreas	Pancrea
25	chr7:104968200-104986800	Weak transcription	Gastric	stomach
26	chr7:104970000-104979800	Weak transcription	Brain Angular Gyrus	brain
27	chr7:104970200-104976600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:104970800-104977800	Enhancers	Dnd41	blood
29	chr7:104971200-104973600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr7:104971600-104973000	Weak transcription	GM12878-XiMat	blood
31	chr7:104972200-104973000	Enhancers	Right Ventricle	heart
32	chr7:104972200-104973600	Enhancers	Esophagus	oesophagus
33	chr7:104972200-104973800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:104972200-104983200	Weak transcription	A549	lung
35	chr7:104972400-104972600	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
36	chr7:104972400-104972800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr7:104972400-104973000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:104972400-104973000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr7:104972400-104973000	Weak transcription	Lung	lung
40	chr7:104972400-104973200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:104972400-104973200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr7:104972400-104973200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr7:104972400-104973400	Enhancers	Primary T cells fromperipheralblood	blood
44	chr7:104972400-104973600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr7:104972400-104973600	Enhancers	Fetal Muscle Leg	muscle
46	chr7:104972400-104983200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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