Variant report

Variant	rs1822304
Chromosome Location	chr1:146647083-146647084
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:146647037-146647200	MCF10A-Er-Src	breast:	n/a	n/a
2	POLR2A	chr1:146646897-146647207	HepG2	liver:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:146642791..146647744-chr1:146694916..146698486,10	MCF-7	breast:
2	chr1:146638044..146647556-chr1:146707628..146717159,48	MCF-7	breast:
3	chr1:146638562..146647588-chr1:146711453..146720391,22	K562	blood:
4	chr1:146644917..146647495-chr1:146694467..146696944,2	K562	blood:
5	chr1:146637222..146651713-chr1:146712141..146718911,44	MCF-7	breast:
6	chr1:146640645..146647502-chr1:146711418..146719354,29	K562	blood:

No data

Variant related genes	Relation type
PDIA3P1	TF binding region
ENSG00000271721	TF binding region
PRKAB2	TF binding region
ENSG00000236806	Chromatin interaction
ENSG00000131778	Chromatin interaction
ENSG00000131781	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12046706	0.97[ASN][1000 genomes]
rs12144722	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1372820	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17159914	0.97[ASN][1000 genomes]
rs1932977	0.91[ASN][1000 genomes]
rs2077749	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2883434	0.98[ASN][1000 genomes]
rs4558036	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4950382	0.98[ASN][1000 genomes]
rs6593745	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6660507	0.93[ASN][1000 genomes]
rs718369	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs720609	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7523021	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7525703	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7527894	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7538682	0.93[ASN][1000 genomes]
rs7548475	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757753	chr1:145883119-146697542	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv872251	chr1:146152553-146803630	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS 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 miRNA target site	95 gene(s)	inside rSNPs	diseases
3	nsv872252	chr1:146471863-147398135	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
4	nsv999546	chr1:146507577-147356574	Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
5	nsv535123	chr1:146507577-147356574	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
6	nsv492188	chr1:146507649-147381479	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
7	nsv916754	chr1:146507711-147417736	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription 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	113 gene(s)	inside rSNPs	diseases
8	nsv547673	chr1:146510112-147398135	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
9	nsv547674	chr1:146522722-147396797	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS 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 miRNA target site	111 gene(s)	inside rSNPs	diseases
10	nsv998341	chr1:146531446-147384720	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
11	nsv535124	chr1:146531446-147384720	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
12	nsv1003493	chr1:146531446-147389944	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
13	nsv998209	chr1:146543722-147384720	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
14	nsv535126	chr1:146543722-147384720	Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
15	nsv872255	chr1:146550780-146969712	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
16	nsv872256	chr1:146556596-147410973	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
17	nsv1012331	chr1:146603479-147384720	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer 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	49 gene(s)	inside rSNPs	diseases
18	nsv535131	chr1:146603479-147384720	Genic enhancers Strong transcription Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS 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	49 gene(s)	inside rSNPs	diseases
19	nsv1009943	chr1:146618929-146893851	Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
20	nsv535132	chr1:146618929-146893851	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
21	nsv872257	chr1:146643555-146724923	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription 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	23 gene(s)	inside rSNPs	diseases
22	nsv437047	chr1:146643555-146841602	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs1822304	CHD1L	cis	Whole Blood	GTEx
rs1822304	RP11-337C18.8	cis	Nerve Tibial	GTEx
rs1822304	RP11-337C18.8	cis	Thyroid	GTEx
rs1822304	CHD1L	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146645000-146649600	Weak transcription	Esophagus	oesophagus
2	chr1:146645000-146649600	Weak transcription	Lung	lung
3	chr1:146645200-146649800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr1:146645400-146648000	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr1:146645400-146649000	Weak transcription	HSMM	muscle
6	chr1:146645400-146649600	Weak transcription	Aorta	Aorta
7	chr1:146645400-146649600	Weak transcription	Ovary	ovary
8	chr1:146645400-146649600	Weak transcription	Thymus	Thymus
9	chr1:146645400-146664400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:146645400-146674800	Weak transcription	Gastric	stomach
11	chr1:146645600-146647600	Weak transcription	Fetal Muscle Leg	muscle
12	chr1:146645600-146649200	Weak transcription	Fetal Intestine Large	intestine
13	chr1:146645600-146649400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:146645600-146649400	Weak transcription	Primary hematopoietic stem cells	blood
15	chr1:146645600-146649400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr1:146645600-146649400	Weak transcription	Psoas Muscle	Psoas
17	chr1:146645600-146649400	Weak transcription	HMEC	breast
18	chr1:146645600-146649600	Weak transcription	Pancreas	Pancrea
19	chr1:146645600-146649600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr1:146645600-146649600	Weak transcription	Spleen	Spleen
21	chr1:146645600-146649800	Weak transcription	Fetal Lung	lung
22	chr1:146645600-146650200	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr1:146645600-146651800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr1:146645600-146661400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:146645800-146648400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr1:146645800-146648600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:146645800-146648800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr1:146645800-146649000	Weak transcription	NHDF-Ad	bronchial
29	chr1:146645800-146649600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:146645800-146649800	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr1:146645800-146649800	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr1:146645800-146675200	Weak transcription	Primary B cells from peripheral blood	blood
33	chr1:146646000-146647600	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr1:146646000-146648000	Weak transcription	Primary B cells from cord blood	blood
35	chr1:146646000-146648000	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr1:146646000-146649000	Weak transcription	NHEK	skin
37	chr1:146646000-146649200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:146646000-146649200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr1:146646000-146649400	Weak transcription	Fetal Kidney	kidney
40	chr1:146646000-146649400	Weak transcription	HUVEC	blood vessel
41	chr1:146646000-146649400	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr1:146646000-146649600	Weak transcription	Liver	Liver
43	chr1:146646000-146649600	Weak transcription	Left Ventricle	heart
44	chr1:146646000-146650200	Weak transcription	Brain Cingulate Gyrus	brain
45	chr1:146646000-146651600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr1:146646000-146655400	Weak transcription	Brain Anterior Caudate	brain
47	chr1:146646000-146656000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr1:146646000-146661200	Weak transcription	Brain Angular Gyrus	brain
49	chr1:146646200-146647600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:146646200-146648000	Weak transcription	Fetal Brain Female	brain

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