Variant report

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:157934538..157936208-chr1:158094108..158095787,2	K562	blood:
2	chr1:158094423..158095037-chr1:178971848..178972362,2	MCF-7	breast:
3	chr1:158094446..158095158-chr1:178971800..178972330,2	MCF-7	breast:
4	chr1:157922938..157923487-chr1:158094554..158095205,2	K562	blood:
5	chr1:157933178..157934221-chr1:158094451..158095320,3	K562	blood:
6	chr1:157933586..157934715-chr1:158094214..158095272,4	MCF-7	breast:
7	chr1:157933076..157934542-chr1:158094256..158095566,6	MCF-7	breast:
8	chr1:157939529..157940163-chr1:158094494..158095209,2	MCF-7	breast:
9	chr1:157848033..157848539-chr1:158094531..158095213,2	K562	blood:
10	chr1:157550095..157550692-chr1:158094281..158095121,2	MCF-7	breast:
11	chr1:157961485..157962628-chr1:158094515..158095728,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000163518	Chromatin interaction

rSNPs within LD-proxies of this variant (count:4)

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	nsv999542	chr1:158015715-158368132	Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 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	chr1:158092600-158095000	Enhancers	Fetal Kidney	kidney
2	chr1:158092600-158095600	Enhancers	HMEC	breast
3	chr1:158092800-158094800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:158092800-158094800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:158093400-158095000	Enhancers	NHEK	skin
6	chr1:158093600-158094800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:158093600-158094800	Enhancers	Hela-S3	cervix
8	chr1:158093800-158094800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr1:158093800-158095600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr1:158093800-158097600	Enhancers	Fetal Thymus	thymus
11	chr1:158094000-158094800	Enhancers	H1 Cell Line	embryonic stem cell
12	chr1:158094000-158094800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:158094000-158094800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:158094000-158094800	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr1:158094000-158095000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr1:158094000-158096800	Enhancers	Thymus	Thymus
17	chr1:158094400-158095400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:158094400-158099600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr1:158094600-158094800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr1:158094600-158094800	Enhancers	Fetal Brain Male	brain

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