Variant report

Variant	rs4492614
Chromosome Location	chr1:154769561-154769562
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:154767709..154770416-chr1:154785808..154787544,2	MCF-7	breast:
2	chr1:154721999..154724952-chr1:154768870..154770453,2	MCF-7	breast:
3	chr1:154764756..154767197-chr1:154768149..154770805,2	MCF-7	breast:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1131820	1.00[CHD][hapmap]
rs12058931	1.00[CHB][hapmap]
rs12729486	1.00[CHB][hapmap]
rs16836525	1.00[JPT][hapmap]
rs4845392	1.00[CHD][hapmap]
rs954785	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948413	chr1:153974621-154797272	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
2	nsv532579	chr1:154548165-155262692	Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	575 gene(s)	inside rSNPs	diseases
3	nsv427797	chr1:154559115-154933717	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv470740	chr1:154568683-154796895	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS 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	18 gene(s)	inside rSNPs	diseases
5	nsv464050	chr1:154568683-154801247	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	nsv547958	chr1:154568683-154801247	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv872452	chr1:154750989-154769561	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:154764600-154770000	Weak transcription	Brain Angular Gyrus	brain
2	chr1:154764600-154773800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr1:154764600-154778400	Weak transcription	Right Atrium	heart
4	chr1:154764600-154779400	Weak transcription	Spleen	Spleen
5	chr1:154764800-154772200	Weak transcription	Fetal Stomach	stomach
6	chr1:154764800-154782600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr1:154765000-154775200	Weak transcription	Brain Substantia Nigra	brain
8	chr1:154765400-154772400	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr1:154765600-154775600	Weak transcription	Brain Hippocampus Middle	brain
10	chr1:154765800-154775800	Weak transcription	Brain Anterior Caudate	brain
11	chr1:154767600-154769800	Enhancers	Fetal Thymus	thymus
12	chr1:154767800-154769800	Enhancers	Fetal Muscle Leg	muscle
13	chr1:154768200-154769600	Enhancers	Thymus	Thymus
14	chr1:154768400-154769600	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr1:154768600-154769600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr1:154768600-154769600	Enhancers	HMEC	breast
17	chr1:154768600-154769600	Bivalent Enhancer	NHEK	skin
18	chr1:154768800-154769600	Enhancers	HSMM	muscle
19	chr1:154768800-154769800	Enhancers	HSMMtube	muscle
20	chr1:154769200-154773800	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr1:154769400-154770600	Strong transcription	GM12878-XiMat	blood
22	chr1:154769400-154771800	Weak transcription	Fetal Brain Female	brain
23	chr1:154769400-154772200	Weak transcription	Fetal Muscle Trunk	muscle
24	chr1:154769400-154776000	Weak transcription	Brain Cingulate Gyrus	brain

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