Variant report

Variant	rs190610833
Chromosome Location	chr1:57577092-57577093
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer 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	20 gene(s)	inside rSNPs	diseases
2	nsv428752	chr1:57455083-57605082	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv461628	chr1:57463326-57816489	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv546305	chr1:57463326-57816489	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv526087	chr1:57576438-57579610	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57551400-57622000	Weak transcription	Fetal Intestine Small	intestine
2	chr1:57571600-57577600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr1:57573400-57577400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:57574200-57578000	Enhancers	Fetal Heart	heart
5	chr1:57574400-57577600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:57575000-57580600	Weak transcription	Left Ventricle	heart
7	chr1:57575000-57581600	Weak transcription	Right Atrium	heart
8	chr1:57575600-57580400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:57576200-57577600	Enhancers	Rectal Smooth Muscle	rectum
10	chr1:57576200-57584800	Weak transcription	Colon Smooth Muscle	Colon
11	chr1:57576600-57577400	Enhancers	Fetal Stomach	stomach
12	chr1:57576800-57577200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:57576800-57577200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr1:57576800-57579800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:57577000-57577200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:57577000-57577400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr1:57577000-57578200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:57577000-57578200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr1:57577000-57578200	Enhancers	HMEC	breast
20	chr1:57577000-57578600	Weak transcription	NHEK	skin
21	chr1:57577000-57578800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr1:57577000-57579800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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