Variant report

Variant	rs2622862
Chromosome Location	chr1:103412924-103412925
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 125 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10047106	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1026660	0.87[EUR][1000 genomes]
rs10493987	1.00[CEU][hapmap]
rs10747433	0.95[AFR][1000 genomes]
rs10747435	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs10782915	1.00[CEU][hapmap]
rs10782916	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs10782917	0.87[AMR][1000 genomes]
rs10782920	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs10874676	0.87[AMR][1000 genomes]
rs11164647	1.00[CEU][hapmap];0.92[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1241167	0.87[EUR][1000 genomes]
rs1337179	0.87[AMR][1000 genomes]
rs1337180	0.87[AMR][1000 genomes]
rs1337192	1.00[CEU][hapmap]
rs1415350	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs1463040	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1463043	0.87[EUR][1000 genomes]
rs1463044	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1463047	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1538047	0.87[AMR][1000 genomes]
rs1538048	0.87[AMR][1000 genomes]
rs1564141	1.00[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1564142	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1626950	0.84[YRI][hapmap]
rs1676488	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1676490	0.81[EUR][1000 genomes]
rs1676492	1.00[AMR][1000 genomes]
rs1676503	1.00[CEU][hapmap];0.87[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1676504	1.00[CEU][hapmap];0.88[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17101127	1.00[CEU][hapmap]
rs17127490	1.00[CEU][hapmap]
rs1763351	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1763360	0.87[EUR][1000 genomes]
rs1841834	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1966958	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2061709	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2184879	0.87[AMR][1000 genomes]
rs2199553	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2615976	1.00[CEU][hapmap];0.92[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2615978	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2615984	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2615985	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2615990	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2615991	1.00[EUR][1000 genomes]
rs2615994	1.00[CEU][hapmap];0.88[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2616000	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs2616008	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2616009	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2616012	1.00[EUR][1000 genomes]
rs2616013	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs2622836	0.87[EUR][1000 genomes]
rs2622837	0.87[EUR][1000 genomes]
rs2622841	1.00[CEU][hapmap]
rs2622849	1.00[CEU][hapmap];0.96[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2622861	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2622863	1.00[EUR][1000 genomes]
rs2622864	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2622867	1.00[CEU][hapmap]
rs2622868	1.00[CEU][hapmap]
rs2622883	1.00[EUR][1000 genomes]
rs2786124	1.00[CEU][hapmap]
rs2929161	1.00[CEU][hapmap]
rs2929162	1.00[CEU][hapmap]
rs3102057	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs3126210	1.00[EUR][1000 genomes]
rs3126211	1.00[EUR][1000 genomes]
rs3126212	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs3126213	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs3126215	1.00[CEU][hapmap]
rs3861743	0.87[AMR][1000 genomes]
rs3908855	1.00[CEU][hapmap]
rs4013869	0.87[AMR][1000 genomes]
rs4357546	0.87[AMR][1000 genomes]
rs4480381	0.87[AMR][1000 genomes]
rs4908279	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6577342	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs6577353	1.00[CEU][hapmap]
rs6667609	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs6674148	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs6700031	0.87[AMR][1000 genomes]
rs7519039	0.87[AMR][1000 genomes]
rs7523020	0.87[AMR][1000 genomes]
rs7523441	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs7531081	1.00[CEU][hapmap]
rs7541571	0.87[AMR][1000 genomes]
rs7544444	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs7544816	1.00[CEU][hapmap]
rs9434362	0.87[EUR][1000 genomes]
rs981961	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs984023	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs992098	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs992099	1.00[CEU][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522922	chr1:103305021-103764640	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv870600	chr1:103336601-103548497	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv871809	chr1:103339272-103459537	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv871732	chr1:103339272-103466917	Genic enhancers Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv871475	chr1:103339272-103548497	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv462728	chr1:103342392-103455217	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv546930	chr1:103342392-103455217	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv870487	chr1:103349419-103466917	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv871019	chr1:103350903-103466917	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv870881	chr1:103352451-103416690	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv870952	chr1:103352451-103432687	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv871807	chr1:103352451-103450196	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv871335	chr1:103352451-103459537	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv870644	chr1:103352451-103466917	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	nsv871741	chr1:103352451-103517428	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv871078	chr1:103352451-103548497	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv871194	chr1:103354138-103416690	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv871970	chr1:103354138-103450196	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
19	nsv871494	chr1:103354138-103466917	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
20	nsv462761	chr1:103356168-103455217	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
21	nsv546933	chr1:103356168-103455217	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
22	nsv870607	chr1:103362909-103528128	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
23	nsv532548	chr1:103381480-103431911	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
24	nsv871840	chr1:103384610-103455217	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
25	nsv870995	chr1:103384610-103548497	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
26	nsv870701	chr1:103393457-103455217	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
27	nsv871929	chr1:103393457-103466917	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
28	nsv871372	chr1:103403752-103564540	Strong transcription Enhancers Active TSS Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
29	nsv546934	chr1:103404384-103450196	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
30	nsv871067	chr1:103407999-103509323	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
31	nsv871736	chr1:103409100-103548497	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
32	nsv870521	chr1:103409558-103466917	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103369600-103498600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:103386200-103482000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:103397800-103414200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:103400200-103424400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:103400200-103444200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:103400200-103462000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr1:103400800-103444200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:103405800-103444200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:103407400-103426000	Weak transcription	NH-A	brain
10	chr1:103407400-103426600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr1:103412600-103417000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:103412600-103421400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:103412800-103424800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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