Variant report

Variant	rs10889361
Chromosome Location	chr1:63183043-63183044
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:63163600-63186600	Weak transcription	HepG2	liver
2	chr1:63171200-63186800	Weak transcription	Fetal Stomach	stomach
3	chr1:63171400-63186400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:63172000-63186600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:63172000-63186600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:63174000-63186800	Weak transcription	Fetal Intestine Small	intestine
7	chr1:63178400-63186200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr1:63178400-63186400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr1:63178400-63186600	Weak transcription	Fetal Muscle Leg	muscle
10	chr1:63178800-63190000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr1:63179000-63186200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr1:63182000-63186800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr1:63182400-63186000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr1:63182400-63186400	Weak transcription	Stomach Mucosa	stomach
15	chr1:63182400-63186600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr1:63182400-63186600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr1:63182400-63187200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr1:63182600-63188000	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr1:63182800-63186200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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