Variant report

Variant	rs7543077
Chromosome Location	chr1:93282528-93282529
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:93282322..93284805-chr1:93286517..93288170,2	K562	blood:
2	chr1:93277281..93280109-chr1:93281216..93283835,2	MCF-7	breast:
3	chr1:93243993..93246087-chr1:93282223..93283796,2	K562	blood:

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10218670	0.89[CEU][hapmap]
rs10735782	0.80[CEU][hapmap]
rs10747448	0.89[CEU][hapmap]
rs10747450	0.80[CEU][hapmap]
rs10782940	0.80[CEU][hapmap]
rs10782944	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10874728	0.80[CEU][hapmap]
rs10874729	0.80[CEU][hapmap]
rs10874731	0.80[CEU][hapmap]
rs10874742	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11164804	0.80[CEU][hapmap]
rs11164808	0.89[CEU][hapmap]
rs11164813	0.80[CEU][hapmap]
rs11164821	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11164845	1.00[CHB][hapmap]
rs12029026	0.85[ASN][1000 genomes]
rs1337109	0.89[CEU][hapmap]
rs1411706	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1415294	0.80[CEU][hapmap]
rs1467559	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1538029	0.80[CEU][hapmap]
rs1556564	0.80[CEU][hapmap]
rs1556565	0.89[CEU][hapmap]
rs1610319	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1929138	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1932966	0.80[CEU][hapmap]
rs1977225	0.85[EUR][1000 genomes]
rs1977227	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1977228	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1977229	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2025100	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2065916	0.80[CEU][hapmap]
rs2095268	0.88[CEU][hapmap]
rs2107520	0.80[CEU][hapmap]
rs2107521	0.89[CEU][hapmap]
rs2244005	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2244496	0.80[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2391179	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2391192	0.81[EUR][1000 genomes]
rs2391193	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2391199	0.89[CEU][hapmap]
rs2774940	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2774941	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs2774943	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2811599	1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs2811602	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2989014	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35054144	0.89[CEU][hapmap]
rs3790445	0.80[CEU][hapmap]
rs3790446	0.80[CEU][hapmap]
rs4240962	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4847221	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4847222	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4847247	0.80[CEU][hapmap]
rs4847363	0.89[CEU][hapmap]
rs4847370	0.89[CEU][hapmap]
rs6604003	0.80[CEU][hapmap]
rs6604010	0.89[CEU][hapmap]
rs6604015	0.89[CEU][hapmap]
rs6604018	0.80[CEU][hapmap]
rs6604025	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6659942	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6661600	0.80[CEU][hapmap]
rs6671421	0.80[CEU][hapmap]
rs6685705	0.89[CEU][hapmap]
rs6687994	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6696636	0.80[CEU][hapmap]
rs6703467	0.80[CEU][hapmap]
rs7416169	0.80[CEU][hapmap]
rs7513624	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7513815	0.89[CEU][hapmap]
rs7514716	0.89[CEU][hapmap]
rs7516141	0.80[CEU][hapmap]
rs7526582	0.80[CEU][hapmap]
rs7527343	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7527356	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7529332	0.80[CEU][hapmap]
rs7529630	0.89[CEU][hapmap]
rs7532731	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7540407	0.89[CEU][hapmap]
rs7541829	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7543112	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7543327	0.80[CEU][hapmap]
rs7543964	0.89[CEU][hapmap];1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs7551340	0.90[ASN][1000 genomes]
rs927339	0.80[CEU][hapmap]
rs932637	0.80[CEU][hapmap]
rs9439920	0.80[CEU][hapmap]
rs9439924	0.90[ASN][1000 genomes]
rs945724	0.80[CEU][hapmap]
rs9662515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs976208	0.80[CEU][hapmap]

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	nsv1008602	chr1:93176811-93640808	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv530047	chr1:93273425-93308213	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93274800-93283600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:93281200-93284000	Enhancers	Fetal Intestine Large	intestine
3	chr1:93281400-93284200	Enhancers	Fetal Intestine Small	intestine
4	chr1:93281800-93284000	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr1:93281800-93284000	Enhancers	Stomach Mucosa	stomach
6	chr1:93281800-93284200	Enhancers	HepG2	liver
7	chr1:93282000-93284200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr1:93282200-93283600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr1:93282400-93283000	Weak transcription	Colonic Mucosa	Colon
10	chr1:93282400-93283000	Weak transcription	Duodenum Mucosa	Duodenum
11	chr1:93282400-93284000	Enhancers	Liver	Liver

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