Variant report

Variant	rs7816935
Chromosome Location	chr8:67520786-67520787
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	chr8:67378110..67380525-chr8:67519992..67522222,2	MCF-7	breast:
2	chr8:67468999..67471572-chr8:67518826..67521712,2	MCF-7	breast:
3	chr8:67442224..67445363-chr8:67520078..67522956,3	MCF-7	breast:
4	chr8:67422088..67426308-chr8:67518696..67523583,8	MCF-7	breast:
5	chr8:67416381..67419252-chr8:67519039..67521783,2	MCF-7	breast:
6	chr8:67371423..67376205-chr8:67520601..67527002,8	MCF-7	breast:
7	chr8:67424089..67425027-chr8:67520588..67521105,2	MCF-7	breast:
8	chr8:67516028..67518138-chr8:67520100..67522413,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000147576	Chromatin interaction
ENSG00000169085	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv831346	chr8:67486555-67675324	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67474200-67521000	Weak transcription	NHEK	skin
2	chr8:67474200-67523000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr8:67474800-67523200	Weak transcription	NH-A	brain
4	chr8:67481800-67523000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:67488600-67523200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr8:67499400-67520800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr8:67500800-67523400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:67501200-67521200	Weak transcription	NHLF	lung
9	chr8:67506200-67522000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:67509200-67523600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:67509600-67522800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr8:67511400-67524600	Weak transcription	Right Atrium	heart
13	chr8:67513200-67523600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:67514800-67522000	Weak transcription	NHDF-Ad	bronchial
15	chr8:67515200-67522000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr8:67515400-67522600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr8:67515800-67521400	Weak transcription	HUVEC	blood vessel
18	chr8:67516000-67523000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr8:67516800-67522800	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr8:67517800-67522200	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr8:67518000-67521600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr8:67518000-67523000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr8:67518000-67524400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr8:67518200-67521400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr8:67519000-67520800	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr8:67519000-67522600	Enhancers	Primary T cells from cord blood	blood
27	chr8:67519200-67523000	Enhancers	Dnd41	blood
28	chr8:67519400-67521600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr8:67519600-67520800	Enhancers	Fetal Heart	heart
30	chr8:67519600-67521400	Flanking Active TSS	GM12878-XiMat	blood
31	chr8:67519600-67521600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:67519600-67522400	Enhancers	HMEC	breast
33	chr8:67519800-67521000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr8:67520000-67521400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr8:67520000-67521400	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr8:67520000-67522000	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr8:67520200-67521000	Weak transcription	HSMM	muscle
38	chr8:67520200-67521800	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr8:67520200-67523200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr8:67520400-67521400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr8:67520600-67522600	Enhancers	Osteobl	bone
42	chr8:67520600-67522800	Enhancers	A549	lung

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