Variant report

Variant	rs11572521
Chromosome Location	chr1:217081514-217081515
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11572509	1.00[YRI][hapmap]
rs11572511	1.00[YRI][hapmap]
rs4436447	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873179	chr1:217056893-217112871	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv873180	chr1:217073060-217112871	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217062800-217087800	Weak transcription	Fetal Muscle Leg	muscle
2	chr1:217072200-217082800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr1:217076800-217083600	Weak transcription	Brain Anterior Caudate	brain
4	chr1:217077000-217081600	Weak transcription	Gastric	stomach
5	chr1:217077000-217082400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:217078600-217088000	Weak transcription	Right Atrium	heart
7	chr1:217078800-217081600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:217079000-217086400	Weak transcription	Fetal Heart	heart
9	chr1:217079400-217081800	Weak transcription	Fetal Intestine Large	intestine
10	chr1:217080000-217081600	Weak transcription	Duodenum Mucosa	Duodenum
11	chr1:217080000-217082600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:217080000-217082600	Weak transcription	HMEC	breast
13	chr1:217081400-217081600	Enhancers	Small Intestine	intestine
14	chr1:217081400-217082000	Enhancers	Fetal Intestine Small	intestine

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

what's new

Quick links