Variant report

Variant	rs2158902
Chromosome Location	chr7:101658239-101658240
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:101657254..101660021-chr7:101660679..101662867,2	MCF-7	breast:
2	chr7:101656842..101659859-chr7:101660301..101664311,4	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10229930	0.86[ASN][1000 genomes]
rs10229976	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10230051	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10230180	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10233058	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10233402	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10238478	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10248831	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10249047	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10253815	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10259603	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10274188	0.92[ASN][1000 genomes]
rs10953357	0.86[CEU][hapmap];0.86[ASN][1000 genomes]
rs12113453	0.86[ASN][1000 genomes]
rs12534969	0.92[ASN][1000 genomes]
rs13437746	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17487672	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17487797	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17494197	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17494372	0.92[ASN][1000 genomes]
rs28461243	0.92[ASN][1000 genomes]
rs28552411	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs28668902	0.92[ASN][1000 genomes]
rs36118129	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56138360	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs56392048	0.92[ASN][1000 genomes]
rs58598138	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60149252	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs62465593	0.86[ASN][1000 genomes]
rs6465843	0.86[CEU][hapmap];0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6465846	0.86[ASN][1000 genomes]
rs66544039	0.86[ASN][1000 genomes]
rs6942801	0.86[ASN][1000 genomes]
rs6973312	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6973714	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73185860	0.92[ASN][1000 genomes]
rs73405966	0.86[ASN][1000 genomes]
rs7357138	0.86[ASN][1000 genomes]
rs7780375	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7780631	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7780927	0.86[ASN][1000 genomes]
rs7797764	0.85[CEU][hapmap];0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7799663	0.92[ASN][1000 genomes]
rs7805379	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7810030	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024319	chr7:101368299-101668159	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv539047	chr7:101368299-101668159	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1020372	chr7:101420819-101718950	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv482846	chr7:101539981-101707666	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv482521	chr7:101604002-101718950	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv831080	chr7:101629121-101718950	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv981839	chr7:101632578-101663728	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv966867	chr7:101645987-101658423	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv1027574	chr7:101654060-101718950	Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101578200-101671200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:101627000-101671200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:101630000-101668000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr7:101641600-101672000	Weak transcription	K562	blood
5	chr7:101642000-101661600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr7:101642200-101666600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:101642200-101671400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr7:101642200-101671600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:101642200-101674600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr7:101642400-101661800	Weak transcription	Spleen	Spleen
11	chr7:101642400-101668000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr7:101642400-101671200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:101642400-101671400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:101642400-101675400	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr7:101642800-101668000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:101642800-101697600	Weak transcription	Primary B cells from cord blood	blood
17	chr7:101643000-101665200	Weak transcription	Primary B cells from peripheral blood	blood
18	chr7:101643000-101672800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:101643000-101675600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr7:101643200-101666400	Weak transcription	Primary hematopoietic stem cells	blood
21	chr7:101644200-101661800	Weak transcription	Right Atrium	heart
22	chr7:101646800-101671600	Weak transcription	GM12878-XiMat	blood
23	chr7:101647200-101662000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:101648200-101671200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:101648200-101681400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr7:101648200-101688000	Weak transcription	Ovary	ovary
27	chr7:101649000-101666800	Weak transcription	Fetal Muscle Leg	muscle
28	chr7:101649000-101671400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr7:101649200-101667000	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr7:101649400-101666600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr7:101649400-101672800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr7:101649600-101665000	Weak transcription	Lung	lung
33	chr7:101649800-101666800	Weak transcription	Fetal Muscle Trunk	muscle
34	chr7:101649800-101671600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:101650800-101664600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:101652000-101659000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:101652400-101671600	Weak transcription	Pancreas	Pancrea
38	chr7:101652400-101683200	Weak transcription	Right Ventricle	heart
39	chr7:101652600-101667400	Weak transcription	Duodenum Mucosa	Duodenum
40	chr7:101652800-101660200	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr7:101652800-101667200	Weak transcription	Esophagus	oesophagus
42	chr7:101652800-101688400	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr7:101653000-101671400	Weak transcription	Stomach Smooth Muscle	stomach
44	chr7:101653000-101688200	Weak transcription	Colonic Mucosa	Colon
45	chr7:101653200-101661600	Weak transcription	Hela-S3	cervix
46	chr7:101653200-101666000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:101653200-101685200	Weak transcription	HSMMtube	muscle
48	chr7:101653400-101661800	Weak transcription	Fetal Thymus	thymus
49	chr7:101653400-101668000	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr7:101653400-101671600	Weak transcription	Gastric	stomach

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