Variant report

Variant	rs34976996
Chromosome Location	chr10:97035169-97035170
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:97030116..97038568-chr10:97046190..97052064,12	MCF-7	breast:
2	chr10:97033378..97035939-chr10:97049305..97051881,3	MCF-7	breast:
3	chr10:97034466..97036166-chr10:97046747..97048932,2	K562	blood:

Variant related genes	Relation type
ENSG00000107438	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10509685	0.85[ASN][1000 genomes]
rs12765981	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12769370	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12783709	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17453729	0.85[ASN][1000 genomes]
rs17453764	0.85[ASN][1000 genomes]
rs17453855	0.92[ASN][1000 genomes]
rs17526000	0.85[ASN][1000 genomes]
rs1854338	0.92[ASN][1000 genomes]
rs35777379	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35830045	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs45444597	0.92[ASN][1000 genomes]
rs45447693	0.92[ASN][1000 genomes]
rs45493292	0.85[ASN][1000 genomes]
rs45498798	0.85[ASN][1000 genomes]
rs45518536	0.81[ASN][1000 genomes]
rs45533831	0.88[ASN][1000 genomes]
rs45554238	0.85[ASN][1000 genomes]
rs45555036	0.92[ASN][1000 genomes]
rs45562941	0.85[ASN][1000 genomes]
rs45569042	0.81[ASN][1000 genomes]
rs45591738	0.85[ASN][1000 genomes]
rs7912686	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]

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	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	esv15160	chr10:96942869-97074756	Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97016800-97036000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr10:97021400-97036400	Weak transcription	Stomach Smooth Muscle	stomach
3	chr10:97024800-97049400	Weak transcription	Fetal Kidney	kidney
4	chr10:97026800-97036000	Weak transcription	Fetal Lung	lung
5	chr10:97027400-97035800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr10:97028600-97036200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr10:97028600-97036200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr10:97028600-97038200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:97028800-97036000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr10:97029000-97036000	Weak transcription	Fetal Thymus	thymus
11	chr10:97029000-97039200	Weak transcription	Fetal Muscle Leg	muscle
12	chr10:97030600-97036200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr10:97030600-97037800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr10:97030800-97036200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:97031000-97036000	Weak transcription	Gastric	stomach
16	chr10:97031000-97038200	Weak transcription	Fetal Stomach	stomach
17	chr10:97031600-97036200	Weak transcription	Primary B cells from cord blood	blood
18	chr10:97031600-97046600	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr10:97032400-97040800	Enhancers	Stomach Mucosa	stomach
20	chr10:97032600-97036400	Enhancers	Liver	Liver
21	chr10:97032600-97041000	Enhancers	Fetal Intestine Large	intestine
22	chr10:97032600-97043600	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr10:97032800-97035200	Enhancers	Right Ventricle	heart
24	chr10:97032800-97035400	Enhancers	Lung	lung
25	chr10:97032800-97037600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr10:97032800-97039200	Enhancers	Duodenum Mucosa	Duodenum
27	chr10:97032800-97042800	Enhancers	Small Intestine	intestine
28	chr10:97033000-97035400	Enhancers	Colonic Mucosa	Colon
29	chr10:97033000-97038600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr10:97033000-97039800	Enhancers	K562	blood
31	chr10:97033400-97037000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr10:97033400-97037800	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr10:97033400-97039000	Enhancers	Left Ventricle	heart
34	chr10:97033400-97039400	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr10:97033600-97035400	Enhancers	Psoas Muscle	Psoas
36	chr10:97033600-97037800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr10:97033600-97037800	Weak transcription	Colon Smooth Muscle	Colon
38	chr10:97033600-97040000	Enhancers	Adipose Nuclei	Adipose
39	chr10:97033800-97035200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:97033800-97036000	Weak transcription	Primary B cells from peripheral blood	blood
41	chr10:97033800-97037600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr10:97033800-97038000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr10:97033800-97039800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr10:97033800-97041600	Enhancers	NHLF	lung
45	chr10:97033800-97042400	Enhancers	Osteobl	bone
46	chr10:97034000-97035400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr10:97034000-97035400	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr10:97034000-97035400	Enhancers	HepG2	liver
49	chr10:97034000-97035400	Weak transcription	HSMM	muscle
50	chr10:97034000-97035600	Weak transcription	Fetal Heart	heart

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