Variant report

Variant	rs72662984
Chromosome Location	chr4:85511181-85511182
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85505200-85511400	Weak transcription	Ovary	ovary
2	chr4:85505800-85511200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:85505800-85511600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:85507200-85513000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr4:85507800-85516000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:85507800-85518000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:85508000-85511600	Weak transcription	Fetal Heart	heart
8	chr4:85508000-85514000	Weak transcription	Stomach Mucosa	stomach
9	chr4:85508800-85531000	Weak transcription	Pancreas	Pancrea
10	chr4:85509400-85514000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr4:85509400-85514600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr4:85509800-85511600	Weak transcription	NHEK	skin
13	chr4:85510000-85516200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:85510200-85511200	Weak transcription	Fetal Intestine Small	intestine
15	chr4:85510200-85511800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:85510200-85511800	Weak transcription	Duodenum Mucosa	Duodenum
17	chr4:85510400-85511200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr4:85510800-85511400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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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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