Variant report

Variant	rs10275705
Chromosome Location	chr7:103845802-103845803
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:103844120..103846835-chr7:103848105..103849807,2	MCF-7	breast:
2	chr7:103835421..103837340-chr7:103844960..103847432,2	K562	blood:
3	chr5:172756464..172758729-chr7:103845451..103847113,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000113739	Chromatin interaction
ENSG00000164815	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10155973	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10230637	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10232393	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10235201	0.88[AFR][1000 genomes]
rs10241191	0.83[AFR][1000 genomes]
rs10242752	0.81[AFR][1000 genomes]
rs10245622	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10248278	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10250051	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10250235	0.91[AFR][1000 genomes]
rs10251976	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10255806	0.90[AFR][1000 genomes]
rs10260238	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10266337	0.87[AFR][1000 genomes]
rs10267412	0.91[AFR][1000 genomes]
rs10271923	0.91[AFR][1000 genomes]
rs10276243	0.88[AFR][1000 genomes]
rs10277637	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10278320	0.83[AFR][1000 genomes]
rs10279675	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10279892	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10281636	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10281709	0.81[AFR][1000 genomes]
rs10282300	0.83[AFR][1000 genomes]
rs10487184	0.81[AFR][1000 genomes]
rs10487192	0.90[AFR][1000 genomes]
rs11979390	0.81[AFR][1000 genomes]
rs11980018	0.83[AFR][1000 genomes]
rs16873387	0.83[AFR][1000 genomes]
rs16873424	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2385134	0.82[AFR][1000 genomes]
rs28686914	0.83[AFR][1000 genomes]
rs28820003	0.89[AFR][1000 genomes]
rs55749110	0.92[EUR][1000 genomes]
rs55901574	0.94[EUR][1000 genomes]
rs56390129	0.97[EUR][1000 genomes]
rs57278162	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59290626	1.00[EUR][1000 genomes]
rs6948021	0.94[AFR][1000 genomes]
rs6949887	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6954109	0.89[AFR][1000 genomes]
rs6971709	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6975642	0.83[AFR][1000 genomes]
rs73413894	0.87[AFR][1000 genomes]
rs73415704	0.89[AFR][1000 genomes]
rs73415708	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73415709	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73415717	0.90[AFR][1000 genomes]
rs73415735	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73415737	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73415786	0.86[AFR][1000 genomes]
rs73415801	0.81[AFR][1000 genomes]
rs7777446	0.83[AFR][1000 genomes]
rs9655777	0.82[AFR][1000 genomes]
rs9656090	0.83[AFR][1000 genomes]
rs9656093	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019640	chr7:103813522-103884705	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
2	nsv1026481	chr7:103813522-103890770	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
3	esv2762692	chr7:103813522-103890782	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
4	nsv526062	chr7:103817597-103891085	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
5	nsv608065	chr7:103817597-103990755	Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103797200-103847000	Weak transcription	Fetal Heart	heart
2	chr7:103816000-103846200	Weak transcription	Stomach Mucosa	stomach
3	chr7:103832800-103846600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:103839800-103847400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:103840000-103847200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr7:103840000-103847600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr7:103840400-103847800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:103840600-103847800	Weak transcription	Small Intestine	intestine
9	chr7:103841000-103846200	Weak transcription	NHLF	lung
10	chr7:103841800-103846800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:103841800-103846800	Weak transcription	Fetal Intestine Small	intestine
12	chr7:103842400-103847200	Weak transcription	HSMMtube	muscle
13	chr7:103842400-103847400	Weak transcription	Lung	lung
14	chr7:103842600-103846000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr7:103842600-103846200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr7:103842600-103846800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr7:103843200-103846400	Weak transcription	Brain Germinal Matrix	brain
18	chr7:103843600-103846200	Weak transcription	Psoas Muscle	Psoas
19	chr7:103843800-103846000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr7:103843800-103846200	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr7:103843800-103846800	Weak transcription	Colonic Mucosa	Colon
22	chr7:103843800-103846800	Weak transcription	Fetal Stomach	stomach
23	chr7:103843800-103847200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:103843800-103847600	Weak transcription	Aorta	Aorta
25	chr7:103844000-103846200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr7:103844000-103846200	Weak transcription	Brain Angular Gyrus	brain
27	chr7:103844000-103846200	Weak transcription	Fetal Brain Female	brain
28	chr7:103844000-103846400	Weak transcription	Fetal Kidney	kidney
29	chr7:103844000-103846400	Weak transcription	Rectal Smooth Muscle	rectum
30	chr7:103844000-103846800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr7:103844000-103847200	Weak transcription	Left Ventricle	heart
32	chr7:103844000-103847600	Weak transcription	Gastric	stomach
33	chr7:103844200-103846200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr7:103844200-103846200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:103844200-103846200	Weak transcription	Brain Hippocampus Middle	brain
36	chr7:103844200-103846200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr7:103844200-103846200	Weak transcription	Ovary	ovary
38	chr7:103844200-103846200	Weak transcription	Right Ventricle	heart
39	chr7:103844200-103846200	Weak transcription	Thymus	Thymus
40	chr7:103844200-103846200	Weak transcription	Spleen	Spleen
41	chr7:103844200-103846200	Weak transcription	Osteobl	bone
42	chr7:103844200-103846800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr7:103844200-103847000	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr7:103844200-103847200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:103844200-103847200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr7:103844200-103847200	Weak transcription	Fetal Thymus	thymus
47	chr7:103844200-103847400	Weak transcription	Esophagus	oesophagus
48	chr7:103844200-103847400	Weak transcription	Fetal Muscle Trunk	muscle
49	chr7:103844200-103847400	Weak transcription	Fetal Muscle Leg	muscle
50	chr7:103844200-103847400	Weak transcription	Placenta	Placenta

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