Variant report

Variant	rs17751319
Chromosome Location	chr14:77930878-77930879
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	POLR2A	chr14:77930232-77931765	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:77929404..77931486-chr14:77963841..77966397,2	MCF-7	breast:
2	chr14:77787549..77790264-chr14:77928506..77931057,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000212371	TF binding region
AHSA1	TF binding region
ENSG00000100593	Chromatin interaction
ENSG00000100577	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10145609	1.00[CHB][hapmap]
rs1063270	1.00[CHB][hapmap]
rs1063271	1.00[CHB][hapmap]
rs11159268	1.00[CHB][hapmap]
rs11159269	1.00[CHB][hapmap]
rs12433806	0.92[CEU][hapmap];1.00[CHB][hapmap]
rs12435437	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[MEX][hapmap]
rs12436626	0.92[CEU][hapmap];1.00[CHB][hapmap]
rs12887556	1.00[CHB][hapmap]
rs17751370	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17751562	0.92[CEU][hapmap];1.00[CHB][hapmap];0.80[MEX][hapmap]
rs17824238	1.00[ASW][hapmap];1.00[CEU][hapmap];0.86[MEX][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17824298	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17824358	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2142188	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2293802	1.00[JPT][hapmap]
rs2364602	1.00[CHB][hapmap]
rs3742729	0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3742731	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3742732	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3742733	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs3742739	1.00[JPT][hapmap]
rs4531669	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6574383	1.00[CHB][hapmap]
rs8003820	1.00[CHB][hapmap]
rs8007669	1.00[CHB][hapmap]
rs8011528	1.00[CHB][hapmap]
rs8177539	1.00[ASW][hapmap];1.00[CHB][hapmap];0.86[MEX][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	nsv1041985	chr14:77877421-77936969	Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv832835	chr14:77906706-78095207	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17751319	ZDHHC22	cis	lymphoblastoid	seeQTL

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77925600-77936600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:77925800-77936400	Strong transcription	Fetal Muscle Trunk	muscle
3	chr14:77926000-77936200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:77926000-77936200	Strong transcription	HUES6 Cell Line	embryonic stem cell
5	chr14:77926000-77936400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:77926000-77936800	Strong transcription	H9 Cell Line	embryonic stem cell
7	chr14:77926000-77936800	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr14:77926000-77939000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr14:77926200-77932000	Strong transcription	Colonic Mucosa	Colon
10	chr14:77926200-77932200	Strong transcription	Rectal Smooth Muscle	rectum
11	chr14:77926200-77932800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
12	chr14:77926200-77933400	Strong transcription	Fetal Brain Male	brain
13	chr14:77926200-77933800	Strong transcription	Gastric	stomach
14	chr14:77926200-77935400	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr14:77926200-77935600	Strong transcription	HSMM	muscle
16	chr14:77926200-77935800	Strong transcription	H1 Cell Line	embryonic stem cell
17	chr14:77926200-77936000	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr14:77926200-77936000	Strong transcription	NHDF-Ad	bronchial
19	chr14:77926200-77936200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:77926200-77936200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr14:77926200-77936200	Strong transcription	HUES48 Cell Line	embryonic stem cell
22	chr14:77926200-77936200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr14:77926200-77936200	Strong transcription	Fetal Intestine Large	intestine
24	chr14:77926200-77936200	Strong transcription	Placenta	Placenta
25	chr14:77926200-77936200	Strong transcription	Fetal Thymus	thymus
26	chr14:77926200-77936200	Strong transcription	Lung	lung
27	chr14:77926200-77936200	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr14:77926200-77936400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr14:77926200-77936400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr14:77926200-77936400	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr14:77926200-77936400	Strong transcription	Skeletal Muscle Male	skeletal muscle
32	chr14:77926200-77936600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr14:77926200-77936800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr14:77926200-77936800	Strong transcription	Muscle Satellite Cultured Cells	--
35	chr14:77926200-77937000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr14:77926200-77937000	Strong transcription	Fetal Stomach	stomach
37	chr14:77926200-77937000	Strong transcription	Ovary	ovary
38	chr14:77926400-77932200	Weak transcription	Psoas Muscle	Psoas
39	chr14:77926400-77932600	Strong transcription	Primary hematopoietic stem cells	blood
40	chr14:77926400-77933400	Strong transcription	Fetal Lung	lung
41	chr14:77926400-77933600	Strong transcription	NHEK	skin
42	chr14:77926400-77935800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr14:77926400-77935800	Strong transcription	Fetal Intestine Small	intestine
44	chr14:77926400-77936000	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr14:77926400-77936000	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr14:77926400-77936000	Strong transcription	HSMMtube	muscle
47	chr14:77926400-77936200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr14:77926400-77936200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr14:77926400-77936200	Strong transcription	Duodenum Mucosa	Duodenum
50	chr14:77926400-77936200	Strong transcription	Fetal Kidney	kidney

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