Variant report

Variant	rs17179204
Chromosome Location	chr14:38014928-38014929
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:38013025..38015360-chr14:38033181..38036117,2	MCF-7	breast:
2	chr14:37992935..37996265-chr14:38014500..38016971,3	MCF-7	breast:
3	chr14:38011441..38015766-chr14:38062652..38065926,9	MCF-7	breast:
4	chr14:38010426..38020494-chr14:38050537..38062032,33	MCF-7	breast:
5	chr14:38014910..38017892-chr14:38018379..38020104,3	MCF-7	breast:
6	chr14:38011817..38019831-chr14:38060493..38066722,23	MCF-7	breast:
7	chr14:38012929..38015442-chr14:38030781..38032707,2	MCF-7	breast:
8	chr14:38014337..38017689-chr14:38019804..38021819,4	MCF-7	breast:
9	chr14:38013523..38020726-chr14:38055776..38060374,10	MCF-7	breast:
10	chr14:38013794..38017816-chr14:38049871..38055560,6	MCF-7	breast:

No data

No data

No data

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

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17106851	0.89[CEU][hapmap]
rs17106852	0.91[CEU][hapmap]
rs17179162	0.91[CEU][hapmap]
rs17768411	0.91[CEU][hapmap];1.00[AFR][1000 genomes]
rs17768417	0.91[CEU][hapmap]
rs17768423	0.91[CEU][hapmap]
rs55751336	1.00[AFR][1000 genomes]
rs56077070	1.00[AFR][1000 genomes]
rs991786	0.91[CEU][hapmap];1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530038	chr14:37590543-38336191	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv901639	chr14:37743583-38038468	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv564349	chr14:37890433-38034434	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv901641	chr14:37939401-38040755	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38008000-38021000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:38008200-38017800	Weak transcription	Aorta	Aorta
3	chr14:38010800-38016000	Weak transcription	Left Ventricle	heart
4	chr14:38013600-38015600	Enhancers	HepG2	liver
5	chr14:38013800-38021200	Weak transcription	Right Ventricle	heart
6	chr14:38013800-38023200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr14:38014200-38015800	Enhancers	A549	lung
8	chr14:38014600-38015600	Enhancers	Liver	Liver
9	chr14:38014600-38035800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr14:38014800-38015800	Weak transcription	NHDF-Ad	bronchial

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links