Variant report

Variant	rs10761208
Chromosome Location	chr9:96072452-96072453
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:96065577..96067663-chr9:96072266..96075048,2	K562	blood:
2	chr9:96071537..96077428-chr9:96212026..96217506,11	MCF-7	breast:
3	chr9:96067941..96071129-chr9:96072035..96075014,3	MCF-7	breast:
4	chr9:95856938..95860270-chr9:96071224..96075475,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000165233	Chromatin interaction
ENSG00000188938	Chromatin interaction
ENSG00000165238	Chromatin interaction
ENSG00000223446	Chromatin interaction
ENSG00000048828	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10733747	0.97[EUR][1000 genomes]
rs10761206	0.87[TSI][hapmap];0.97[EUR][1000 genomes]
rs10821104	0.97[EUR][1000 genomes]
rs1111776	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12341311	0.89[ASW][hapmap]
rs12350787	1.00[CHB][hapmap]
rs12683662	0.95[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs12684392	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12684553	0.97[EUR][1000 genomes]
rs1331588	0.85[TSI][hapmap]
rs1343631	0.97[EUR][1000 genomes]
rs16909005	1.00[MEX][hapmap]
rs16909013	0.89[ASW][hapmap]
rs17532098	1.00[CHB][hapmap]
rs1889338	0.91[YRI][hapmap]
rs1891970	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1931365	0.94[EUR][1000 genomes]
rs1931366	0.97[EUR][1000 genomes]
rs1931367	0.87[TSI][hapmap];0.97[EUR][1000 genomes]
rs1931368	0.97[EUR][1000 genomes]
rs1936401	1.00[EUR][1000 genomes]
rs2151714	0.91[YRI][hapmap]
rs2169756	0.95[YRI][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2991376	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs2995999	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs3001449	0.92[AFR][1000 genomes]
rs3001453	0.83[GIH][hapmap]
rs3847306	1.00[CEU][hapmap];0.85[GIH][hapmap]
rs4147136	0.94[EUR][1000 genomes]
rs4548243	0.91[YRI][hapmap]
rs4743908	0.97[EUR][1000 genomes]
rs4743909	0.94[EUR][1000 genomes]
rs4743913	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs4743914	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs4744209	0.94[EUR][1000 genomes]
rs4744210	0.97[EUR][1000 genomes]
rs4744214	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs56161352	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6479458	0.85[GIH][hapmap]
rs6479470	0.87[TSI][hapmap];0.94[EUR][1000 genomes]
rs6479472	1.00[EUR][1000 genomes]
rs6479473	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7020940	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7021187	1.00[EUR][1000 genomes]
rs7025514	1.00[CEU][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes]
rs7025611	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs7031917	1.00[CEU][hapmap];0.94[YRI][hapmap];0.85[AFR][1000 genomes]
rs7042028	0.91[EUR][1000 genomes]
rs7042492	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7044229	0.97[AFR][1000 genomes]
rs73651384	0.85[AFR][1000 genomes]
rs7853075	0.92[YRI][hapmap];0.88[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7856268	1.00[EUR][1000 genomes]
rs7866298	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7872608	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9657693	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv893580	chr9:95855100-96099377	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv430082	chr9:95905745-96095045	Genic enhancers Enhancers Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv893582	chr9:95963114-96116937	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv893583	chr9:95996573-96091688	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv893584	chr9:96002983-96116937	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96033400-96077200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:96033600-96072800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr9:96055600-96080200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr9:96056400-96079800	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr9:96061400-96075000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr9:96061600-96079000	Weak transcription	Gastric	stomach
7	chr9:96063800-96088600	Weak transcription	Right Atrium	heart
8	chr9:96065000-96079200	Weak transcription	Colonic Mucosa	Colon
9	chr9:96065200-96080000	Weak transcription	Spleen	Spleen
10	chr9:96065400-96073200	Strong transcription	Fetal Intestine Small	intestine
11	chr9:96066000-96082800	Weak transcription	Fetal Thymus	thymus
12	chr9:96067200-96072600	Strong transcription	Pancreas	Pancrea
13	chr9:96067200-96081200	Weak transcription	Fetal Heart	heart
14	chr9:96067400-96074200	Weak transcription	HepG2	liver
15	chr9:96067600-96073600	Strong transcription	Fetal Intestine Large	intestine
16	chr9:96067600-96079200	Weak transcription	Right Ventricle	heart
17	chr9:96067600-96086800	Weak transcription	Fetal Brain Male	brain
18	chr9:96067800-96086800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr9:96068200-96086200	Weak transcription	Brain Anterior Caudate	brain
20	chr9:96068400-96082400	Weak transcription	Brain Angular Gyrus	brain
21	chr9:96068400-96100400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr9:96068600-96073800	Strong transcription	Fetal Brain Female	brain
23	chr9:96068600-96079200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr9:96068600-96080200	Weak transcription	Left Ventricle	heart
25	chr9:96068800-96080800	Weak transcription	Psoas Muscle	Psoas
26	chr9:96068800-96082600	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr9:96069200-96079400	Weak transcription	Fetal Muscle Leg	muscle
28	chr9:96069400-96079600	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr9:96069400-96080000	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr9:96070000-96075000	Weak transcription	Colon Smooth Muscle	Colon
31	chr9:96070200-96073600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr9:96070600-96073000	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr9:96070600-96075000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr9:96070600-96087800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr9:96070800-96077200	Weak transcription	Stomach Smooth Muscle	stomach
36	chr9:96071400-96074600	Weak transcription	Duodenum Mucosa	Duodenum
37	chr9:96071400-96075000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr9:96071400-96078800	Weak transcription	Brain Germinal Matrix	brain
39	chr9:96071400-96079000	Weak transcription	Fetal Stomach	stomach
40	chr9:96072200-96072600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr9:96072200-96072600	Strong transcription	Sigmoid Colon	Sigmoid Colon
42	chr9:96072200-96073600	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr9:96072400-96073200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell

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