Variant report

Variant	rs17029177
Chromosome Location	chr4:100509648-100509649
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10516454	1.00[YRI][hapmap]
rs17029309	1.00[YRI][hapmap]
rs6828637	1.00[YRI][hapmap]

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	nsv879656	chr4:99976646-100533722	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv933074	chr4:100460951-100630600	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	esv3410965	chr4:100509154-100511252	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv3377330	chr4:100509589-100510392	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100506200-100509800	Enhancers	Fetal Intestine Small	intestine
2	chr4:100506200-100516000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:100506800-100510800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:100507800-100510400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr4:100507800-100533800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr4:100508600-100509800	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr4:100508600-100509800	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr4:100508800-100510400	Weak transcription	Liver	Liver
9	chr4:100508800-100514000	Strong transcription	HepG2	liver
10	chr4:100509000-100511400	Weak transcription	Duodenum Mucosa	Duodenum
11	chr4:100509000-100516000	Weak transcription	Aorta	Aorta
12	chr4:100509400-100509800	Enhancers	Fetal Heart	heart
13	chr4:100509600-100509800	Enhancers	Ovary	ovary
14	chr4:100509600-100510600	Genic enhancers	Fetal Intestine Large	intestine

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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

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