Variant report

Variant	rs884897
Chromosome Location	chr7:97798117-97798118
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	chr7:97797557..97798288-chr7:97870683..97871212,2	MCF-7	breast:
2	chr3:18799324..18800175-chr7:97797657..97798586,2	MCF-7	breast:
3	chr7:97650735..97651576-chr7:97797624..97798555,4	MCF-7	breast:
4	chr7:97650523..97652025-chr7:97797434..97798619,17	K562	blood:
5	chr7:97650523..97651440-chr7:97797679..97798686,5	MCF-7	breast:
6	chr7:97734947..97737685-chr7:97796527..97798334,3	K562	blood:
7	chr7:97735592..97736320-chr7:97797651..97798233,3	K562	blood:
8	chr7:97759468..97762062-chr7:97796586..97798629,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000164715	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1039057	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11761896	0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11762771	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11768678	0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11772060	0.87[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11773169	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1532380	0.85[EUR][1000 genomes]
rs17169325	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2394824	0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4729404	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4729408	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55761857	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55765204	0.89[AMR][1000 genomes]
rs56006208	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs56034325	0.85[EUR][1000 genomes]
rs56088922	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56174823	0.89[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs56389625	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58911561	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62479768	0.92[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs62479773	0.89[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs62479795	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62479797	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[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	nsv1031371	chr7:97312452-98070538	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv3500384	chr7:97527787-98015382	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
3	esv3500386	chr7:97527787-98015382	Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
4	nsv1017481	chr7:97597641-98041043	Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	nsv539031	chr7:97597641-98041043	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
6	nsv1019531	chr7:97653880-98034129	Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv539032	chr7:97653880-98034129	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	esv1816676	chr7:97676259-97868033	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv831066	chr7:97726879-97890550	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv1033029	chr7:97773232-98017992	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
11	nsv539033	chr7:97773232-98017992	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs884897	DKFZP434B0335	Cis_1M	lymphoblastoid	RTeQTL
rs884897	AKAP8	trans	lymphoblastoid	RTeQTL

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97763400-97801000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:97763400-97821000	Weak transcription	NHLF	lung
3	chr7:97763600-97814200	Weak transcription	Osteobl	bone
4	chr7:97763600-97815800	Weak transcription	HSMM	muscle
5	chr7:97764000-97806200	Weak transcription	Psoas Muscle	Psoas
6	chr7:97765800-97840800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr7:97766600-97798400	Weak transcription	HSMMtube	muscle
8	chr7:97768800-97807000	Weak transcription	Stomach Mucosa	stomach
9	chr7:97772400-97821600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr7:97775600-97803600	Weak transcription	K562	blood
11	chr7:97781800-97808200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:97782400-97803600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr7:97782400-97819000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr7:97782400-97822000	Weak transcription	Fetal Kidney	kidney
15	chr7:97782400-97839800	Weak transcription	Fetal Brain Male	brain
16	chr7:97782600-97807400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr7:97784600-97815000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:97785000-97801000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:97785000-97804000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr7:97785200-97818600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr7:97785400-97804600	Weak transcription	NHDF-Ad	bronchial
22	chr7:97785400-97804800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:97785600-97804200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:97786400-97800800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr7:97786800-97800400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:97786800-97801200	Weak transcription	Placenta	Placenta
27	chr7:97787200-97799400	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr7:97787400-97800200	Weak transcription	Fetal Muscle Trunk	muscle
29	chr7:97787400-97800800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:97787400-97801000	Weak transcription	Fetal Muscle Leg	muscle
31	chr7:97787400-97808200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr7:97787400-97822000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:97787800-97800400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr7:97788200-97800400	Weak transcription	Fetal Thymus	thymus
35	chr7:97788400-97800200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:97789000-97800000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr7:97789000-97803800	Weak transcription	Brain Germinal Matrix	brain
38	chr7:97789200-97798600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr7:97789200-97800800	Weak transcription	Aorta	Aorta
40	chr7:97789200-97800800	Weak transcription	Thymus	Thymus
41	chr7:97789200-97801000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:97789200-97801000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr7:97789200-97803600	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr7:97789200-97803600	Weak transcription	Fetal Brain Female	brain
45	chr7:97789200-97829400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr7:97789400-97798800	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr7:97789400-97801000	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr7:97789400-97802200	Weak transcription	Left Ventricle	heart
49	chr7:97789400-97803600	Weak transcription	Primary hematopoietic stem cells	blood
50	chr7:97789600-97801600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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