Variant report

Variant	rs2525722
Chromosome Location	chr7:120606438-120606439
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	POLR2A	chr7:120605786-120606742	K562	blood:	n/a	n/a
2	POLR2A	chr7:120606124-120606667	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:120548487..120550613-chr7:120604026..120606804,2	K562	blood:
2	chr7:120605041..120607016-chr7:120723328..120726105,2	K562	blood:
3	chr7:120588468..120596180-chr7:120604298..120610010,9	MCF-7	breast:

Variant related genes	Relation type
ING3	TF binding region
ENSG00000071243	Chromatin interaction
ENSG00000212628	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10258025	0.81[EUR][1000 genomes]
rs11363	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13881	0.94[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2074576	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2074577	0.95[CEU][hapmap]
rs2215786	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs2215789	0.94[CEU][hapmap]
rs2244863	0.95[CEU][hapmap]
rs2244865	0.95[CEU][hapmap]
rs2525711	0.94[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2525712	0.95[CEU][hapmap]
rs2525713	0.95[CEU][hapmap]
rs2525714	0.94[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2525715	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs2525716	0.94[CEU][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2525717	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2525718	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2525719	1.00[CEU][hapmap]
rs2525720	0.94[CEU][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2525723	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2525724	0.94[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2525725	0.94[CEU][hapmap];0.97[EUR][1000 genomes]
rs2525726	0.94[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2525728	0.94[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2525731	0.94[EUR][1000 genomes]
rs2525732	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2525733	0.94[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2525734	0.94[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2525735	0.94[CEU][hapmap];0.82[EUR][1000 genomes]
rs2525738	0.94[CEU][hapmap]
rs2525739	0.94[CEU][hapmap]
rs2525740	0.94[CEU][hapmap]
rs2721350	0.94[CEU][hapmap];0.97[EUR][1000 genomes]
rs2721351	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2721363	0.85[CEU][hapmap]
rs2721366	0.94[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2721368	0.94[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2721370	0.94[CEU][hapmap];0.97[EUR][1000 genomes]
rs2721372	1.00[CEU][hapmap]
rs3944026	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs41688	0.95[CEU][hapmap]
rs41691	0.94[CEU][hapmap]
rs41692	0.94[CEU][hapmap]
rs41694	0.94[CEU][hapmap]
rs41697	0.94[CEU][hapmap]
rs41703	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs41704	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs4727917	0.82[CEU][hapmap]
rs6966297	0.94[CEU][hapmap];0.88[EUR][1000 genomes]
rs6973457	0.94[CEU][hapmap];0.85[EUR][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	esv1818826	chr7:120405335-120622836	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv831114	chr7:120595624-120804510	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2525722	TSPAN12	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120591600-120606600	Weak transcription	Lung	lung
2	chr7:120591600-120608000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:120591600-120608000	Weak transcription	Esophagus	oesophagus
4	chr7:120591600-120608000	Weak transcription	Gastric	stomach
5	chr7:120591600-120608000	Weak transcription	Spleen	Spleen
6	chr7:120591600-120611200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr7:120591600-120612800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:120591600-120613200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr7:120591600-120613200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:120591600-120627800	Weak transcription	Pancreas	Pancrea
11	chr7:120591800-120618600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr7:120592200-120611000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr7:120592400-120607800	Weak transcription	HSMMtube	muscle
14	chr7:120592400-120608000	Weak transcription	Psoas Muscle	Psoas
15	chr7:120592400-120614800	Weak transcription	Small Intestine	intestine
16	chr7:120592400-120617000	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr7:120592400-120618600	Weak transcription	Right Ventricle	heart
18	chr7:120592400-120621600	Weak transcription	Aorta	Aorta
19	chr7:120592400-120628000	Weak transcription	Stomach Mucosa	stomach
20	chr7:120594400-120608000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:120594800-120609000	Weak transcription	NH-A	brain
22	chr7:120595000-120610800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:120595200-120608000	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr7:120595600-120608000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:120595600-120608000	Weak transcription	Fetal Intestine Small	intestine
26	chr7:120596000-120608000	Weak transcription	HepG2	liver
27	chr7:120596400-120608000	Weak transcription	Colonic Mucosa	Colon
28	chr7:120596600-120607800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr7:120596600-120607800	Weak transcription	NHDF-Ad	bronchial
30	chr7:120596600-120608000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr7:120596800-120606600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr7:120596800-120607800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:120596800-120607800	Weak transcription	A549	lung
34	chr7:120597400-120608000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:120597400-120608000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr7:120597600-120606600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr7:120597600-120608000	Weak transcription	Fetal Stomach	stomach
38	chr7:120598600-120607800	Weak transcription	Brain Angular Gyrus	brain
39	chr7:120599200-120606600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr7:120599400-120606600	Weak transcription	Brain Germinal Matrix	brain
41	chr7:120599600-120606600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr7:120599600-120616200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr7:120600400-120606600	Weak transcription	Thymus	Thymus
44	chr7:120600400-120609000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:120601800-120613000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr7:120602400-120606600	Weak transcription	Colon Smooth Muscle	Colon
47	chr7:120602600-120617200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:120602800-120615800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr7:120603000-120618000	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr7:120603200-120618000	Strong transcription	Fetal Thymus	thymus

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