Variant report

Variant	rs762833
Chromosome Location	chr4:2790801-2790802
allele	C/T
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	HNF4A	chr4:2790504-2790831	HepG2	liver:	n/a	chr4:2790721-2790736

No.	Distal block	Cell Line	Cell type
1	chr4:2756774..2759335-chr4:2790160..2792143,2	K562	blood:
2	chr4:2790052..2809152-chr4:2930639..2948075,83	MCF-7	breast:
3	chr4:2788496..2791956-chr4:2791998..2795194,4	K562	blood:
4	chr4:2788574..2792648-chr4:2935718..2939026,4	K562	blood:
5	chr4:2753714..2768807-chr4:2789818..2806638,47	MCF-7	breast:
6	chr4:2756774..2758480-chr4:2789820..2791660,2	K562	blood:

Variant related genes	Relation type
SH3BP2	TF binding region
ENSG00000109736	Chromatin interaction
ENSG00000168884	Chromatin interaction
ENSG00000087266	Chromatin interaction
ENSG00000249673	Chromatin interaction
ENSG00000087269	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1263449	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1271256	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs172998	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs182820	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs190160	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs231334	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs390288	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs408102	0.93[ASN][1000 genomes]
rs743691	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs762834	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948659	chr4:1828867-2815632	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
2	nsv1005116	chr4:2633935-2812340	Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv878444	chr4:2689449-2861090	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv470002	chr4:2701098-2836628	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv878445	chr4:2704046-2831383	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv878446	chr4:2710644-2810634	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv878447	chr4:2723531-2831383	Flanking Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Enhancers Strong transcription Active 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	19 gene(s)	inside rSNPs	diseases
8	nsv516797	chr4:2723531-2836628	Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
9	nsv878448	chr4:2723531-2846799	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer 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 target site	22 gene(s)	inside rSNPs	diseases
10	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
11	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer 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	63 gene(s)	inside rSNPs	diseases
12	nsv878449	chr4:2744480-2831383	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv1002517	chr4:2747905-2822017	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	nsv878450	chr4:2760222-2861090	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
15	nsv967941	chr4:2765555-2802771	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
16	nsv593435	chr4:2770772-2881256	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv878451	chr4:2785556-2856687	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers 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	14 gene(s)	inside rSNPs	diseases
18	nsv878452	chr4:2789184-2830076	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2784000-2791600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr4:2786600-2794800	Enhancers	Primary B cells from cord blood	blood
3	chr4:2786800-2794800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr4:2786800-2794800	Enhancers	Primary B cells from peripheral blood	blood
5	chr4:2787000-2791400	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr4:2787200-2791000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr4:2787200-2791600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr4:2787200-2792000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr4:2787400-2791600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr4:2787400-2794800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr4:2787800-2794400	Enhancers	Spleen	Spleen
12	chr4:2787800-2794800	Enhancers	Fetal Muscle Leg	muscle
13	chr4:2788000-2791200	Enhancers	Fetal Muscle Trunk	muscle
14	chr4:2788000-2794200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:2788200-2793600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:2788400-2791600	Enhancers	Right Ventricle	heart
17	chr4:2788800-2791400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr4:2789200-2793000	Enhancers	Liver	Liver
19	chr4:2789400-2791200	Enhancers	Fetal Intestine Large	intestine
20	chr4:2789600-2791600	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr4:2789600-2792200	Weak transcription	K562	blood
22	chr4:2789800-2791000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr4:2789800-2793000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr4:2789800-2793000	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr4:2789800-2793400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:2789800-2793400	Weak transcription	Pancreas	Pancrea
27	chr4:2789800-2793400	Weak transcription	Stomach Mucosa	stomach
28	chr4:2789800-2793800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr4:2789800-2793800	Weak transcription	A549	lung
30	chr4:2789800-2794800	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr4:2789800-2794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr4:2790000-2791400	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr4:2790000-2791600	Enhancers	GM12878-XiMat	blood
34	chr4:2790000-2792000	Enhancers	Primary T cells fromperipheralblood	blood
35	chr4:2790000-2793800	Weak transcription	Gastric	stomach
36	chr4:2790000-2794000	Weak transcription	Hela-S3	cervix
37	chr4:2790000-2794400	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr4:2790000-2794800	Weak transcription	Brain Substantia Nigra	brain
39	chr4:2790200-2791000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr4:2790200-2791200	Weak transcription	Esophagus	oesophagus
41	chr4:2790200-2792200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr4:2790200-2793400	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr4:2790200-2795400	Weak transcription	Fetal Lung	lung
44	chr4:2790400-2791600	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr4:2790400-2792200	Weak transcription	Adipose Nuclei	Adipose
46	chr4:2790400-2792800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr4:2790400-2793000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr4:2790400-2793000	Weak transcription	Colonic Mucosa	Colon
49	chr4:2790400-2793800	Weak transcription	Lung	lung
50	chr4:2790400-2794000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links