Variant report

No.	Distal block	Cell Line	Cell type
1	chr14:65288996..65290569-chr14:65296688..65298749,2	MCF-7	breast:
2	chr14:65296488..65300322-chr14:65306337..65310294,4	K562	blood:
3	chr14:65291589..65293730-chr14:65297377..65299857,2	K562	blood:

Variant related genes	Relation type
ENSG00000070182	Chromatin interaction

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1006613	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17826231	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs189087	1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs229613	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs229614	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs229615	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs229617	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72726215	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8017631	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3693408	chr14:65292670-65358576	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65296400-65308600	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr14:65296600-65298600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr14:65296600-65300200	Enhancers	Fetal Muscle Leg	muscle
4	chr14:65297200-65301200	Enhancers	Psoas Muscle	Psoas
5	chr14:65297200-65304000	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr14:65297400-65298000	Enhancers	Right Atrium	heart
7	chr14:65297400-65298200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr14:65297400-65298400	Enhancers	Right Ventricle	heart
9	chr14:65297400-65298600	Enhancers	Left Ventricle	heart
10	chr14:65297400-65299200	Enhancers	Fetal Heart	heart
11	chr14:65297400-65300000	Enhancers	K562	blood
12	chr14:65297600-65298200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:65297600-65298200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:65297600-65298400	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr14:65297800-65298200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr14:65297800-65298200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr14:65297800-65298200	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr14:65297800-65298400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr14:65297800-65298400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr14:65297800-65298400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr14:65297800-65298600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:65297800-65298600	Enhancers	Fetal Muscle Trunk	muscle

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