Variant report

Variant	rs7138035
Chromosome Location	chr12:104657527-104657528
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	EP300	chr12:104657152-104658189	SK-N-SH	brain:	n/a	n/a
2	FOS	chr12:104657474-104658164	MCF10A-Er-Src	breast:	n/a	n/a
3	GATA3	chr12:104657046-104658213	SK-N-SH	brain:	n/a	n/a
4	TCF12	chr12:104656930-104658314	SK-N-SH	brain:	n/a	n/a
5	POLR2A	chr12:104657268-104657606	SK-N-SH	brain:	n/a	n/a
6	POLR2A	chr12:104657223-104657743	SK-N-SH	brain:	n/a	n/a
7	PBX3	chr12:104657122-104658098	SK-N-SH	brain:	n/a	chr12:104657311-104657320
8	FOS	chr12:104657495-104658087	MCF10A-Er-Src	breast:	n/a	n/a
9	MYC	chr12:104657340-104658053	MCF10A-Er-Src	breast:	n/a	n/a
10	POLR2A	chr12:104657340-104658045	HL-60	blood:	n/a	n/a
11	SPI1	chr12:104657375-104657951	HL-60	blood:	n/a	n/a
12	JUND	chr12:104657147-104658162	SK-N-SH	brain:	n/a	n/a
13	NFIC	chr12:104657175-104658023	SK-N-SH	brain:	n/a	n/a
14	GATA3	chr12:104657048-104658232	SK-N-SH	brain:	n/a	n/a
15	MAX	chr12:104657222-104657773	SK-N-SH	brain:	n/a	n/a
16	PBX3	chr12:104657016-104658202	SK-N-SH	brain:	n/a	chr12:104657311-104657320
17	NFIC	chr12:104657139-104658213	SK-N-SH	brain:	n/a	n/a
18	TCF12	chr12:104656931-104658292	SK-N-SH	brain:	n/a	n/a
19	MYC	chr12:104657429-104658007	MCF10A-Er-Src	breast:	n/a	n/a
20	STAT3	chr12:104657525-104658030	MCF10A-Er-Src	breast:	n/a	n/a
21	EP300	chr12:104657192-104657753	SK-N-SH_RA	brain:	n/a	n/a
22	FOS	chr12:104657527-104658026	MCF10A-Er-Src	breast:	n/a	n/a
23	GATA2	chr12:104657206-104657669	SH-SY5Y	brain:	n/a	n/a
24	EP300	chr12:104657137-104657746	SK-N-SH_RA	brain:	n/a	n/a
25	GATA3	chr12:104657100-104657609	SH-SY5Y	brain:	n/a	n/a
26	MAX	chr12:104657511-104657748	NB4	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:104654376..104656180-chr12:104656602..104658713,2	K562	blood:

Variant related genes	Relation type
RPL18AP3	TF binding region

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10735392	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10735393	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs10735395	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10745995	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10745996	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10778323	0.84[CEU][hapmap]
rs10861204	0.91[CEU][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11111943	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11111955	0.81[ASN][1000 genomes]
rs17035504	0.82[CEU][hapmap]
rs17202862	0.82[CEU][hapmap]
rs4129598	0.91[CEU][hapmap]
rs4246264	0.82[CEU][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4246269	0.91[CEU][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4246270	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4246271	0.91[CEU][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4388968	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4447242	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4502051	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4545635	0.91[CEU][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4614534	0.91[CEU][hapmap]
rs4630362	0.91[CEU][hapmap]
rs4964227	0.82[CEU][hapmap]
rs4964228	0.82[CEU][hapmap]
rs4964257	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4964260	0.91[CEU][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4964270	0.81[ASN][1000 genomes]
rs4964288	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4964627	0.82[CEU][hapmap]
rs4964741	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4964752	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4964761	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4964779	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4964784	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6419386	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6539137	0.90[CEU][hapmap]
rs6539138	0.84[CEU][hapmap]
rs7132418	0.82[CEU][hapmap]
rs7138317	0.82[CEU][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7139336	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7294997	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7298613	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7299866	0.91[CEU][hapmap]
rs7305872	0.81[AMR][1000 genomes]
rs73181916	0.83[AMR][1000 genomes]
rs7957725	0.82[CEU][hapmap]
rs7958851	0.83[ASN][1000 genomes]
rs7962423	0.91[CEU][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7969351	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7969380	0.87[ASN][1000 genomes]
rs7975161	0.84[ASN][1000 genomes]
rs7978101	0.81[AMR][1000 genomes]
rs9738614	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9739826	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9739833	0.91[CEU][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899493	chr12:104548613-104703228	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv899494	chr12:104561521-104806232	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1046606	chr12:104606617-104763734	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1038609	chr12:104613847-104764981	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv541587	chr12:104613847-104764981	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104652000-104669600	Weak transcription	Hela-S3	cervix
2	chr12:104652800-104673000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr12:104656200-104658200	Enhancers	A549	lung
4	chr12:104656200-104658400	Enhancers	HMEC	breast
5	chr12:104656400-104658200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:104656400-104658200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:104656600-104658200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr12:104656800-104657600	Enhancers	Fetal Thymus	thymus
9	chr12:104656800-104658000	Enhancers	Stomach Mucosa	stomach
10	chr12:104656800-104658200	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr12:104656800-104658200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr12:104656800-104658200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr12:104656800-104658200	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr12:104656800-104658600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr12:104657000-104658200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr12:104657000-104658200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr12:104657000-104658200	Enhancers	HSMM	muscle
18	chr12:104657000-104658200	Enhancers	NHLF	lung
19	chr12:104657000-104658400	Enhancers	HSMMtube	muscle
20	chr12:104657000-104658800	Enhancers	NHDF-Ad	bronchial
21	chr12:104657200-104657800	Enhancers	H9 Cell Line	embryonic stem cell
22	chr12:104657200-104658200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr12:104657200-104658200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:104657200-104658200	Flanking Active TSS	NHEK	skin
25	chr12:104657200-104658400	Enhancers	Muscle Satellite Cultured Cells	--
26	chr12:104657400-104657600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr12:104657400-104658000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:104657400-104658000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr12:104657400-104658000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:104657400-104658000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:104657400-104658000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:104657400-104658200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr12:104657400-104658200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr12:104657400-104658200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr12:104657400-104658200	Enhancers	NH-A	brain
36	chr12:104657400-104658400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr12:104657400-104658400	Enhancers	Osteobl	bone

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