Variant report

Variant	rs10943103
Chromosome Location	chr6:74278499-74278500
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:74277679..74279983-chr6:74283539..74285265,2	K562	blood:
2	chr6:74229266..74230904-chr6:74278283..74280721,3	MCF-7	breast:
3	chr6:74274687..74279711-chr6:74293912..74296161,4	K562	blood:
4	chr6:74227140..74231865-chr6:74277040..74281960,6	K562	blood:
5	chr6:74273534..74278713-chr6:74287099..74290342,5	K562	blood:
6	chr6:74275602..74279787-chr6:74300038..74304050,3	MCF-7	breast:
7	chr6:74227140..74235678-chr6:74271460..74282263,27	K562	blood:
8	chr6:74223467..74225709-chr6:74277005..74278629,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000229862	Chromatin interaction
ENSG00000156508	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11963033	1.00[CEU][hapmap];0.88[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12190444	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12191112	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12193628	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12197170	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12198839	0.91[EUR][1000 genomes]
rs12199142	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12199577	1.00[CEU][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12205957	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12205991	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12212315	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28365878	1.00[EUR][1000 genomes]
rs3857464	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3857465	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4302642	1.00[EUR][1000 genomes]
rs56104432	0.96[EUR][1000 genomes]
rs56375536	1.00[EUR][1000 genomes]
rs72947408	1.00[EUR][1000 genomes]
rs72947410	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3410973	chr6:73716033-74419545	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv886158	chr6:74126084-74436825	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
3	nsv1027968	chr6:74155378-74521923	Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
4	nsv538305	chr6:74155378-74521923	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
5	nsv1017716	chr6:74173173-74401162	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
6	nsv1023250	chr6:74189642-74605976	Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
7	nsv538306	chr6:74189642-74605976	Strong transcription Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS 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	172 gene(s)	inside rSNPs	diseases
8	nsv463153	chr6:74229258-74290291	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	141 gene(s)	inside rSNPs	diseases
9	nsv603693	chr6:74229258-74290291	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	141 gene(s)	inside rSNPs	diseases
10	nsv527357	chr6:74253266-74325403	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv603694	chr6:74275405-74365807	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74274600-74278600	Enhancers	Placenta	Placenta
2	chr6:74276000-74279200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr6:74276400-74280200	Weak transcription	Fetal Heart	heart
4	chr6:74276400-74287800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:74276600-74279600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr6:74277000-74279000	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr6:74277000-74279600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:74277200-74278800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:74277200-74278800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr6:74277200-74279000	Weak transcription	NH-A	brain
11	chr6:74277200-74280600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr6:74277200-74280600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr6:74277200-74280600	Weak transcription	HSMM	muscle
14	chr6:74277200-74280800	Weak transcription	Fetal Muscle Leg	muscle
15	chr6:74277200-74280800	Weak transcription	K562	blood
16	chr6:74277200-74287200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr6:74277200-74287400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr6:74277200-74287600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:74277200-74288600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:74277400-74278800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr6:74277400-74279000	Enhancers	HepG2	liver
22	chr6:74277400-74280400	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr6:74277400-74280600	Weak transcription	HSMMtube	muscle
24	chr6:74277400-74280800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr6:74277800-74280600	Weak transcription	A549	lung
26	chr6:74277800-74280800	Weak transcription	Liver	Liver
27	chr6:74278000-74278800	Enhancers	Placenta Amnion	Placenta Amnion
28	chr6:74278200-74279000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:74278200-74279000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:74278200-74280800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:74278200-74288600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:74278400-74281400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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