Variant report

Variant	rs59057489
Chromosome Location	chr6:45892704-45892705
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ELF1	chr6:45892437-45892907	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:45623457..45625814-chr6:45890186..45892755,2	MCF-7	breast:
2	chr6:44620218..44622571-chr6:45890865..45893250,2	MCF-7	breast:

Variant related genes	Relation type
CLIC5	TF binding region

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs35618986	0.92[AMR][1000 genomes]
rs3777545	0.92[AMR][1000 genomes]

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	nsv532024	chr6:45475088-45982640	Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1021917	chr6:45879064-45898314	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45866600-45898400	Weak transcription	Colonic Mucosa	Colon
2	chr6:45881200-45908000	Weak transcription	Duodenum Mucosa	Duodenum
3	chr6:45882400-45898400	Weak transcription	Fetal Intestine Large	intestine
4	chr6:45886800-45910600	Weak transcription	Psoas Muscle	Psoas
5	chr6:45887400-45896600	Weak transcription	Fetal Intestine Small	intestine
6	chr6:45887800-45892800	Enhancers	GM12878-XiMat	blood
7	chr6:45888400-45892800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr6:45889200-45897200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:45890000-45898000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr6:45890000-45898000	Weak transcription	Right Atrium	heart
11	chr6:45890000-45898000	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr6:45890400-45892800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:45890600-45894800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:45890600-45901600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:45891000-45898400	Weak transcription	Fetal Kidney	kidney
16	chr6:45891200-45892800	Enhancers	Placenta	Placenta
17	chr6:45891400-45898000	Weak transcription	Fetal Heart	heart
18	chr6:45891600-45898400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr6:45891800-45896400	Weak transcription	Right Ventricle	heart
20	chr6:45891800-45896600	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr6:45892000-45893200	Weak transcription	Left Ventricle	heart
22	chr6:45892000-45895600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:45892200-45894000	Weak transcription	Fetal Stomach	stomach
24	chr6:45892200-45895000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr6:45892200-45897400	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr6:45892200-45897400	Weak transcription	Osteobl	bone
27	chr6:45892600-45892800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr6:45892600-45894600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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