Variant report

Variant	rs7180126
Chromosome Location	chr15:40279581-40279582
allele	A/C
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	FOXA1	chr15:40279367-40279750	HepG2	liver:	n/a	n/a
2	FOXA2	chr15:40279528-40279725	HepG2	liver:	n/a	n/a
3	FOXA1	chr15:40279357-40279806	HepG2	liver:	n/a	n/a
4	FOXA1	chr15:40279293-40279714	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
EIF2AK4	TF binding region

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12050879	0.96[ASN][1000 genomes]
rs12915244	0.84[JPT][hapmap]
rs16970164	0.89[JPT][hapmap]
rs17721809	0.89[ASN][1000 genomes]
rs2307104	0.85[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2412452	0.81[EUR][1000 genomes]
rs28514956	0.90[EUR][1000 genomes]
rs2917836	0.81[EUR][1000 genomes]
rs34682510	0.94[EUR][1000 genomes]
rs3816901	0.89[JPT][hapmap]
rs516009	0.81[EUR][1000 genomes]
rs558662	0.90[EUR][1000 genomes]
rs8030505	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530816	chr15:40003136-40586792	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv428635	chr15:40274500-40436293	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv516913	chr15:40279581-40280693	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40227400-40283400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:40228200-40323800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr15:40236600-40303000	Weak transcription	Small Intestine	intestine
4	chr15:40249000-40304800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr15:40250000-40294800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr15:40250200-40299600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr15:40260800-40303400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr15:40262600-40293800	Weak transcription	Stomach Mucosa	stomach
9	chr15:40266400-40281800	Weak transcription	K562	blood
10	chr15:40269000-40284800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr15:40269000-40293200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:40269000-40293200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr15:40269200-40282000	Weak transcription	Esophagus	oesophagus
14	chr15:40269200-40283000	Weak transcription	Psoas Muscle	Psoas
15	chr15:40269400-40281600	Weak transcription	Colonic Mucosa	Colon
16	chr15:40269400-40283000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr15:40269600-40282400	Weak transcription	Fetal Brain Male	brain
18	chr15:40269600-40295600	Weak transcription	Fetal Heart	heart
19	chr15:40269800-40285400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr15:40270400-40282400	Weak transcription	Primary B cells from peripheral blood	blood
21	chr15:40276400-40295600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr15:40277600-40287400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr15:40277600-40288000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr15:40277600-40288000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:40277600-40288400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr15:40277600-40294600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr15:40277600-40303600	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr15:40277600-40303800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr15:40277600-40304400	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr15:40277800-40279600	Strong transcription	Aorta	Aorta
31	chr15:40277800-40279600	Strong transcription	Brain Angular Gyrus	brain
32	chr15:40277800-40279600	Strong transcription	Brain Hippocampus Middle	brain
33	chr15:40277800-40279600	Strong transcription	Colon Smooth Muscle	Colon
34	chr15:40277800-40279600	Strong transcription	Fetal Lung	lung
35	chr15:40277800-40279600	Strong transcription	Placenta Amnion	Placenta Amnion
36	chr15:40277800-40279800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr15:40277800-40279800	Strong transcription	Lung	lung
38	chr15:40277800-40281400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr15:40277800-40283800	Strong transcription	HUVEC	blood vessel
40	chr15:40277800-40284200	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr15:40277800-40285800	Strong transcription	Brain Cingulate Gyrus	brain
42	chr15:40277800-40286000	Strong transcription	Brain Anterior Caudate	brain
43	chr15:40277800-40286600	Strong transcription	Skeletal Muscle Male	skeletal muscle
44	chr15:40277800-40286600	Strong transcription	A549	lung
45	chr15:40277800-40286600	Strong transcription	Dnd41	blood
46	chr15:40277800-40286600	Strong transcription	HSMM	muscle
47	chr15:40277800-40286600	Strong transcription	NHDF-Ad	bronchial
48	chr15:40277800-40286600	Strong transcription	NHEK	skin
49	chr15:40277800-40286600	Strong transcription	Osteobl	bone
50	chr15:40277800-40286800	Strong transcription	Muscle Satellite Cultured Cells	--

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