Variant report

Variant	rs55823933
Chromosome Location	chr7:102072689-102072690
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:102072108-102072710	GM18951	blood:	n/a	n/a
2	PML	chr7:102071742-102072758	GM12878	blood:	n/a	n/a
3	POLR2A	chr7:102072127-102072788	HL-60	blood:	n/a	n/a
4	ELF1	chr7:102072056-102072708	MCF-7	breast:	n/a	chr7:102072388-102072401
5	EBF1	chr7:102072243-102072886	GM12878	blood:	n/a	n/a
6	EBF1	chr7:102072196-102072796	GM12878	blood:	n/a	n/a
7	POLR2A	chr7:102072216-102072744	GM12892	blood:	n/a	n/a
8	POLR2A	chr7:102072177-102072706	GM12878	blood:	n/a	n/a
9	POLR2A	chr7:102072132-102072792	Raji	blood:	n/a	n/a
10	YY1	chr7:102072108-102072773	GM12892	blood:	n/a	n/a
11	POLR2A	chr7:102072114-102072785	GM12892	blood:	n/a	n/a
12	POLR2A	chr7:102072112-102072732	GM12891	blood:	n/a	n/a
13	POLR2A	chr7:102071894-102072738	SK-N-MC	brain:	n/a	n/a
14	POLR2A	chr7:102071181-102072804	GM12878	blood:	n/a	n/a
15	PAX5	chr7:102071974-102072806	GM12878	blood:	n/a	chr7:102072236-102072253
16	RCOR1	chr7:102071853-102072818	GM12878	blood:	n/a	n/a
17	SPI1	chr7:102071799-102072728	GM12878	blood:	n/a	n/a
18	RUNX3	chr7:102071300-102072822	GM12878	blood:	n/a	chr7:102072432-102072441 chr7:102072432-102072441
19	POLR2A	chr7:102072056-102072717	GM19193	blood:	n/a	n/a
20	PML	chr7:102072461-102072698	GM12878	blood:	n/a	n/a
21	POLR2A	chr7:102071932-102072697	GM12878	blood:	n/a	n/a
22	MAX	chr7:102071218-102072788	NB4	blood:	n/a	chr7:102071521-102071530
23	POLR2A	chr7:102071949-102072714	GM18505	blood:	n/a	n/a
24	ELF1	chr7:102072083-102072778	GM12878	blood:	n/a	chr7:102072388-102072401
25	RELA	chr7:102071973-102072720	GM19099	blood:	n/a	n/a
26	POLR2A	chr7:102072024-102072740	GM19099	blood:	n/a	n/a
27	POLR2A	chr7:102072165-102072695	GM12878	blood:	n/a	n/a
28	STAT5A	chr7:102071909-102072717	GM12878	blood:	n/a	chr7:102072478-102072490
29	POLR2A	chr7:102072038-102072702	GM12891	blood:	n/a	n/a
30	EP300	chr7:102071904-102072702	GM12878	blood:	n/a	n/a
31	MTA3	chr7:102071138-102073907	GM12878	blood:	n/a	n/a
32	MAX	chr7:102072033-102072793	GM12878	blood:	n/a	n/a
33	SPI1	chr7:102072051-102072732	HL-60	blood:	n/a	n/a
34	POLR2A	chr7:102071980-102072816	GM12878	blood:	n/a	n/a
35	STAT5A	chr7:102071989-102073029	GM12878	blood:	n/a	chr7:102072478-102072490
36	POLR2A	chr7:102071269-102073515	GM12891	blood:	n/a	n/a
37	POLR2A	chr7:102072045-102072713	GM15510	blood:	n/a	n/a
38	RUNX3	chr7:102071897-102072840	GM12878	blood:	n/a	chr7:102072432-102072441 chr7:102072432-102072441
39	POLR2A	chr7:102072111-102072806	HL-60	blood:	n/a	n/a
40	BCLAF1	chr7:102072135-102072741	GM12878	blood:	n/a	n/a
41	CHD2	chr7:102072197-102072730	GM12878	blood:	n/a	n/a
42	POLR2A	chr7:102071905-102075388	GM12878	blood:	n/a	n/a
43	POLR2A	chr7:102071977-102072774	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:102069773..102072990-chr7:102073477..102075231,3	K562	blood:
2	chr7:102063067..102066587-chr7:102070734..102073141,4	MCF-7	breast:
3	chr7:101927893..101931251-chr7:102072337..102075849,4	MCF-7	breast:

Variant related genes	Relation type
ORAI2	TF binding region
ENSG00000239480	Chromatin interaction
ENSG00000160999	Chromatin interaction
ENSG00000160991	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10229440	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1134521	0.95[ASN][1000 genomes]
rs12672177	0.90[ASN][1000 genomes]
rs17135196	0.91[ASN][1000 genomes]
rs2950183	0.85[ASN][1000 genomes]
rs3823656	1.00[ASN][1000 genomes]
rs4584084	1.00[ASN][1000 genomes]
rs55893391	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55953136	1.00[ASN][1000 genomes]
rs56411810	0.91[ASN][1000 genomes]
rs62482947	0.95[ASN][1000 genomes]
rs62482951	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62482952	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62482953	0.99[ASN][1000 genomes]
rs62483800	1.00[ASN][1000 genomes]
rs6958346	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1814780	chr7:101912320-102375950	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv1819566	chr7:101912320-102375950	Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Enhancers 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 miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	esv1822347	chr7:101912320-102375950	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	esv1825708	chr7:101912320-102375950	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
5	esv1842898	chr7:101912320-102375950	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
6	esv1847418	chr7:101912320-102375950	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
7	nsv427798	chr7:101912320-102375950	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
8	nsv428182	chr7:101912320-102375950	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
9	nsv1016563	chr7:101912320-102695860	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
10	nsv1028438	chr7:101912320-102704135	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
11	nsv1029079	chr7:101939998-102112371	Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
12	esv1818954	chr7:101957513-102328097	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	esv1828190	chr7:101966669-102439077	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
14	esv1829377	chr7:101970299-102330884	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
15	nsv831083	chr7:101981005-102295869	Active TSS Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
16	esv1806297	chr7:101981544-102330884	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
17	esv1810415	chr7:101993063-102375950	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
18	esv1811751	chr7:101993063-102375950	Enhancers Genic enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
19	esv1829118	chr7:101993063-102375950	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
20	esv1833155	chr7:101993063-102375950	Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
21	esv1832541	chr7:102072448-102328097	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
22	nsv1025363	chr7:102072448-102471485	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 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	chr7:102050800-102073400	Weak transcription	Psoas Muscle	Psoas
2	chr7:102051200-102073400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:102051400-102074400	Weak transcription	Fetal Heart	heart
4	chr7:102053600-102073200	Weak transcription	Right Atrium	heart
5	chr7:102054000-102073400	Weak transcription	Small Intestine	intestine
6	chr7:102066000-102073400	Weak transcription	HUVEC	blood vessel
7	chr7:102066200-102074000	Weak transcription	Fetal Lung	lung
8	chr7:102066400-102073600	Weak transcription	NHDF-Ad	bronchial
9	chr7:102066600-102073400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr7:102066800-102073200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr7:102067400-102073200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:102067400-102073200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:102067400-102073400	Weak transcription	Aorta	Aorta
14	chr7:102067400-102073400	Weak transcription	NH-A	brain
15	chr7:102067400-102073600	Weak transcription	Hela-S3	cervix
16	chr7:102067600-102073000	Weak transcription	Osteobl	bone
17	chr7:102067600-102073400	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr7:102067800-102073200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr7:102067800-102073200	Weak transcription	HSMMtube	muscle
20	chr7:102067800-102073400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:102067800-102073400	Weak transcription	Left Ventricle	heart
22	chr7:102067800-102073400	Weak transcription	NHLF	lung
23	chr7:102067800-102073600	Weak transcription	Gastric	stomach
24	chr7:102068000-102073000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr7:102068200-102072800	Weak transcription	Stomach Smooth Muscle	stomach
26	chr7:102068200-102073200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr7:102068200-102073200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:102068400-102073200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr7:102068400-102073200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:102068400-102073400	Weak transcription	Dnd41	blood
31	chr7:102068600-102073000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:102068800-102073200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr7:102068800-102073400	Weak transcription	HSMM	muscle
34	chr7:102069200-102073000	Weak transcription	Fetal Stomach	stomach
35	chr7:102069600-102073400	Enhancers	Spleen	Spleen
36	chr7:102069800-102072800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr7:102069800-102073400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
38	chr7:102069800-102073400	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr7:102070000-102073400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr7:102070200-102073600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr7:102070400-102073600	Weak transcription	Lung	lung
42	chr7:102070800-102073200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr7:102070800-102073200	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr7:102071000-102074400	Enhancers	Fetal Brain Male	brain
45	chr7:102071200-102073000	Enhancers	Duodenum Mucosa	Duodenum
46	chr7:102071200-102073200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr7:102071200-102073200	Enhancers	Brain Cingulate Gyrus	brain
48	chr7:102071200-102073400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr7:102071200-102073600	Enhancers	K562	blood
50	chr7:102071400-102073400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links