Variant report

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:39236198..39237902-chr6:39244519..39247184,2	MCF-7	breast:
2	chr6:39234576..39236394-chr6:39278908..39280593,2	MCF-7	breast:
3	chr6:39228773..39231561-chr6:39235112..39238664,3	K562	blood:
4	chr6:39173237..39177206-chr6:39236026..39240576,5	MCF-7	breast:
5	chr6:39195419..39197389-chr6:39235803..39237695,3	K562	blood:
6	chr6:39235849..39239507-chr6:39267408..39272188,7	MCF-7	breast:
7	chr6:39236174..39238959-chr6:39247299..39249650,2	MCF-7	breast:
8	chr6:39233505..39239976-chr6:39262109..39267318,6	MCF-7	breast:
9	chr6:39195043..39199102-chr6:39233396..39239186,7	MCF-7	breast:
10	chr6:39235093..39238743-chr6:39267391..39271695,7	MCF-7	breast:
11	chr6:39167435..39172891-chr6:39233498..39237624,6	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000164626	Chromatin interaction

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs2395718	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58571754	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6910910	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6913790	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7754914	0.98[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	nsv830644	chr6:39116530-39325980	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1022974	chr6:39120271-39277553	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv830645	chr6:39227601-39408310	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:39224400-39238400	Weak transcription	Spleen	Spleen
2	chr6:39231400-39236600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:39231800-39236400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr6:39231800-39236400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr6:39232000-39239800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr6:39233600-39240200	Enhancers	Placenta	Placenta
7	chr6:39234600-39236600	Enhancers	Placenta Amnion	Placenta Amnion
8	chr6:39234600-39236800	Enhancers	H9 Cell Line	embryonic stem cell
9	chr6:39234600-39237000	Enhancers	Fetal Thymus	thymus
10	chr6:39234800-39237800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:39234800-39239000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:39235000-39236600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:39235400-39236800	Enhancers	Thymus	Thymus
14	chr6:39235600-39237000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:39236000-39236600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:39236000-39236800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:39236000-39237000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr6:39236000-39237200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr6:39236000-39241200	Weak transcription	Colonic Mucosa	Colon
20	chr6:39236000-39241400	Weak transcription	Rectal Mucosa Donor 31	rectum

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