Variant report

Variant	rs77169785
Chromosome Location	chr6:113851938-113851939
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916294	chr6:113518489-113904305	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv981078	chr6:113851437-113874497	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:113849600-113852400	Enhancers	HMEC	breast
2	chr6:113850200-113852400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr6:113850200-113852400	Enhancers	NHDF-Ad	bronchial
4	chr6:113850200-113852600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:113850400-113852000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:113850800-113852000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:113851000-113852000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr6:113851000-113852000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr6:113851000-113852000	Weak transcription	NHLF	lung
10	chr6:113851000-113852000	Weak transcription	Osteobl	bone
11	chr6:113851000-113852200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:113851400-113852800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:113851600-113852200	Enhancers	NHEK	skin
14	chr6:113851800-113852000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr6:113851800-113852200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:113851800-113852400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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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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