Variant report

Variant	rs397860823
Chromosome Location	chr1:210847315-210847316
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:210846826..210848354-chr1:210867968..210870812,2	K562	blood:

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873148	chr1:210665583-210994339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv522480	chr1:210779936-210848344	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
3	esv1825229	chr1:210789477-210854976	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
4	nsv873150	chr1:210808270-210893233	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
5	nsv873152	chr1:210820285-210854815	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
6	esv3396391	chr1:210846870-210847345	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210827600-210847600	Weak transcription	HSMM	muscle
2	chr1:210829000-210853400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:210835400-210863200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr1:210837800-210847600	Weak transcription	Pancreas	Pancrea
5	chr1:210837800-210854200	Weak transcription	Fetal Muscle Leg	muscle
6	chr1:210837800-210859800	Weak transcription	Right Ventricle	heart
7	chr1:210838000-210880400	Weak transcription	Gastric	stomach
8	chr1:210838200-210848200	Weak transcription	Left Ventricle	heart
9	chr1:210843600-210855800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:210843800-210857400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:210844000-210847600	Weak transcription	HSMMtube	muscle
12	chr1:210845000-210848400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr1:210845000-210857000	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr1:210845400-210853800	Weak transcription	Fetal Stomach	stomach
15	chr1:210845400-210866000	Weak transcription	Spleen	Spleen
16	chr1:210845800-210857600	Weak transcription	Fetal Intestine Small	intestine
17	chr1:210846000-210865600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr1:210846200-210862400	Weak transcription	Stomach Smooth Muscle	stomach
19	chr1:210846200-210865800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:210846400-210855600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:210846400-210884600	Weak transcription	Ovary	ovary
22	chr1:210847000-210860200	Weak transcription	Muscle Satellite Cultured Cells	--

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