Variant report

Variant	rs17281377
Chromosome Location	chrX:154066470-154066471
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chrX:154061070..154063634-chrX:154065927..154067882,2	K562	blood:
2	X:153635385-153648319..X:154065057-154068472	K562	blood:
3	X:153625659-153635385..X:154065057-154068472	K562	blood:
4	X:154000894-154002691..X:154065057-154068472	H1-hESC	embryonic stem cell:	embryo
5	X:153755323-153771683..X:154065057-154068472	K562	blood:
6	chrX:154064369..154067194-chrX:154067800..154070767,2	K562	blood:
7	X:153967468-153979902..X:154065057-154068472	K562	blood:
8	X:153989469-153994716..X:154065057-154068472	K562	blood:
9	X:154007450-154013157..X:154065057-154068472	K562	blood:
10	X:153586280-153597086..X:154065057-154068472	K562	blood:
11	chrX:154056293..154057860-chrX:154065721..154068695,2	K562	blood:
12	X:154015910-154019964..X:154065057-154068472	H1-hESC	embryonic stem cell:	embryo
13	X:154013320-154015910..X:154065057-154068472	K562	blood:
14	X:154002691-154005706..X:154065057-154068472	K562	blood:
15	X:153994716-154000894..X:154065057-154068472	K562	blood:

No data

No data

No data

Variant related genes	Relation type
ENSG00000196924	Chromatin interaction
ENSG00000160211	Chromatin interaction
ENSG00000073009	Chromatin interaction
ENSG00000160219	Chromatin interaction
ENSG00000147403	Chromatin interaction
ENSG00000102125	Chromatin interaction
ENSG00000203870	Chromatin interaction
ENSG00000206948	Chromatin interaction
ENSG00000207165	Chromatin interaction
ENSG00000130830	Chromatin interaction
ENSG00000130826	Chromatin interaction
ENSG00000206693	Chromatin interaction
ENSG00000013563	Chromatin interaction

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:154064800-154067600	Weak transcription	Adipose Nuclei	Adipose
2	chrX:154065000-154077600	Weak transcription	Brain Anterior Caudate	brain
3	chrX:154065800-154067200	Enhancers	K562	blood
4	chrX:154066000-154085400	Weak transcription	Spleen	Spleen

Quick Search:

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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