Variant report

Variant	rs10281981
Chromosome Location	chr7:98986990-98986991
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:12)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:12 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:98986803-98988142	HL-60	blood:	n/a	n/a
2	POLR2A	chr7:98986841-98986996	GM12878	blood:	n/a	n/a
3	POLR2A	chr7:98986864-98999101	K562	blood:	n/a	n/a
4	POLR2A	chr7:98986762-98988249	K562	blood:	n/a	n/a
5	POLR2A	chr7:98986931-98987121	U87	brain:	n/a	n/a
6	POLR2A	chr7:98986770-98988040	K562	blood:	n/a	n/a
7	POLR2A	chr7:98986935-98987647	HepG2	liver:	n/a	n/a
8	POLR2A	chr7:98986757-98987978	PANC-1	pancreas:	n/a	n/a
9	POLR2A	chr7:98986963-98988248	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr7:98986840-98989273	GM12878	blood:	n/a	n/a
11	POLR2A	chr7:98986956-98988180	A549	lung:	n/a	n/a
12	POLR2A	chr7:98986744-98987125	PFSK-1	brain:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:98970980..98974747-chr7:98986775..98992580,7	MCF-7	breast:
2	chr7:98986172..98988816-chr7:99004808..99007138,3	MCF-7	breast:
3	chr7:98981776..98988825-chr7:99001775..99008244,9	K562	blood:

No data

Variant related genes	Relation type
ARPC1B	TF binding region
ENSG00000106244	Chromatin interaction
ENSG00000130429	Chromatin interaction
ENSG00000106245	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10215758	0.90[LWK][hapmap];1.00[MKK][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10231045	1.00[AMR][1000 genomes]
rs10232946	1.00[AMR][1000 genomes]
rs10234586	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10235168	1.00[AMR][1000 genomes]
rs10237782	1.00[AMR][1000 genomes]
rs10248906	1.00[AMR][1000 genomes]
rs10249095	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10249159	1.00[AMR][1000 genomes]
rs10251931	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10254863	1.00[AMR][1000 genomes]
rs10258918	0.90[LWK][hapmap];1.00[MKK][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10260157	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10260896	0.90[LWK][hapmap];0.83[MKK][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10268692	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10273355	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10274078	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10274095	0.90[LWK][hapmap];1.00[MKK][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10274601	1.00[AMR][1000 genomes]
rs10275948	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28621023	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7779190	1.00[MKK][hapmap];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3433144	chr7:98777878-99060209	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	nsv831068	chr7:98819572-99006481	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv831069	chr7:98948128-99127584	Active TSS Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:98971000-98990400	Weak transcription	Fetal Kidney	kidney
2	chr7:98973400-98987400	Weak transcription	Brain Germinal Matrix	brain
3	chr7:98973400-98987800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr7:98973400-98989800	Weak transcription	Brain Angular Gyrus	brain
5	chr7:98978000-98987000	Weak transcription	Small Intestine	intestine
6	chr7:98978200-98989800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:98978800-98989000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr7:98979000-98989600	Weak transcription	Stomach Mucosa	stomach
9	chr7:98979200-98987000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:98979200-98987000	Weak transcription	HSMM	muscle
11	chr7:98979200-98989600	Weak transcription	Brain Substantia Nigra	brain
12	chr7:98979400-99001800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:98979600-98989800	Weak transcription	Fetal Heart	heart
14	chr7:98979600-98990200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:98979600-98990200	Weak transcription	Right Atrium	heart
16	chr7:98980400-99003800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr7:98980600-98989600	Strong transcription	NHEK	skin
18	chr7:98980800-98990000	Strong transcription	NHLF	lung
19	chr7:98980800-99000600	Strong transcription	Dnd41	blood
20	chr7:98981000-98988400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr7:98981000-98993000	Strong transcription	A549	lung
22	chr7:98981200-98989800	Strong transcription	Fetal Intestine Small	intestine
23	chr7:98981200-98989800	Strong transcription	Thymus	Thymus
24	chr7:98981200-98990000	Strong transcription	K562	blood
25	chr7:98981400-98989800	Strong transcription	Muscle Satellite Cultured Cells	--
26	chr7:98981400-98989800	Strong transcription	Fetal Stomach	stomach
27	chr7:98981600-98989800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:98981800-98988800	Strong transcription	GM12878-XiMat	blood
29	chr7:98981800-98989800	Weak transcription	Fetal Brain Male	brain
30	chr7:98982400-98987200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:98982400-98987400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr7:98982400-98989600	Strong transcription	Spleen	Spleen
33	chr7:98982400-98989800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr7:98982800-98989000	Strong transcription	Fetal Thymus	thymus
35	chr7:98983000-98988600	Strong transcription	Gastric	stomach
36	chr7:98983000-98989400	Strong transcription	Fetal Muscle Leg	muscle
37	chr7:98983000-98989600	Strong transcription	HMEC	breast
38	chr7:98983000-98989600	Strong transcription	HUVEC	blood vessel
39	chr7:98983000-98989800	Strong transcription	Sigmoid Colon	Sigmoid Colon
40	chr7:98983200-98989000	Strong transcription	Pancreas	Pancrea
41	chr7:98983200-98989000	Strong transcription	Right Ventricle	heart
42	chr7:98983200-98989200	Strong transcription	Colonic Mucosa	Colon
43	chr7:98983200-98989400	Strong transcription	Fetal Intestine Large	intestine
44	chr7:98983200-98989800	Strong transcription	Fetal Muscle Trunk	muscle
45	chr7:98983200-98989800	Strong transcription	Lung	lung
46	chr7:98983200-98990000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:98983200-98990000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:98983200-98990000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr7:98983400-98988800	Strong transcription	Stomach Smooth Muscle	stomach
50	chr7:98983400-98989200	Strong transcription	Esophagus	oesophagus

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