Variant report

Variant	rs372101730
Chromosome Location	chr10:119026559-119026560
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3424329	chr10:119026362-119030860	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:119017400-119034000	Weak transcription	Gastric	stomach
2	chr10:119019800-119031200	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr10:119020000-119034000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:119020000-119042600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr10:119020600-119028000	Weak transcription	Thymus	Thymus
6	chr10:119020600-119035000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr10:119020600-119043200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:119020600-119045400	Weak transcription	Fetal Heart	heart
9	chr10:119021400-119043200	Weak transcription	Fetal Intestine Small	intestine
10	chr10:119022600-119042000	Weak transcription	Fetal Intestine Large	intestine
11	chr10:119023000-119031800	Weak transcription	Ovary	ovary
12	chr10:119023800-119043200	Weak transcription	Spleen	Spleen
13	chr10:119025200-119026800	Weak transcription	HepG2	liver
14	chr10:119026000-119027000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:119026000-119032600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr10:119026200-119027000	Weak transcription	Fetal Thymus	thymus
17	chr10:119026200-119031400	Weak transcription	K562	blood
18	chr10:119026400-119029200	Strong transcription	Primary T cells from cord blood	blood

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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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