Variant report

Variant	rs62133443
Chromosome Location	chr2:21502085-21502086
allele	G/T
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	nsv519215	chr2:21473751-21502727	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
2	nsv1011486	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv535602	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv518468	chr2:21489083-21502727	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv3391805	chr2:21502047-21506645	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21492000-21504600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:21493400-21511200	Weak transcription	Aorta	Aorta
3	chr2:21493800-21509000	Weak transcription	K562	blood
4	chr2:21494200-21504800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:21494200-21506200	Weak transcription	Right Atrium	heart
6	chr2:21494600-21504400	Weak transcription	Brain Anterior Caudate	brain
7	chr2:21497800-21504800	Weak transcription	Spleen	Spleen
8	chr2:21498600-21504600	Weak transcription	Brain Angular Gyrus	brain
9	chr2:21499800-21506600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:21500200-21502200	Weak transcription	Fetal Muscle Trunk	muscle
11	chr2:21500200-21502400	Weak transcription	Left Ventricle	heart
12	chr2:21500400-21504400	Weak transcription	Brain Substantia Nigra	brain
13	chr2:21500800-21504400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr2:21501000-21502400	Weak transcription	Fetal Muscle Leg	muscle
15	chr2:21501000-21502600	Weak transcription	Brain Hippocampus Middle	brain
16	chr2:21501400-21504600	Weak transcription	Fetal Intestine Small	intestine
17	chr2:21501600-21502400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr2:21501600-21504000	Weak transcription	Fetal Intestine Large	intestine
19	chr2:21502000-21504000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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