Variant report

Variant	rs10272245
Chromosome Location	chr7:138180275-138180276
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10236035	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10271000	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10279876	1.00[ASN][1000 genomes]
rs11761566	0.85[CEU][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11763093	1.00[ASN][1000 genomes]
rs11773577	1.00[ASN][1000 genomes]
rs12707387	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12707388	0.86[CEU][hapmap];0.93[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13230953	1.00[ASN][1000 genomes]
rs13231375	1.00[ASN][1000 genomes]
rs13242427	1.00[ASN][1000 genomes]
rs3213902	0.92[CEU][hapmap];0.85[YRI][hapmap];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34718165	1.00[ASN][1000 genomes]
rs35558871	1.00[ASN][1000 genomes]
rs35674497	1.00[ASN][1000 genomes]
rs55918517	1.00[ASN][1000 genomes]
rs6467774	0.87[CEU][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6467777	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6467779	0.92[CEU][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6467781	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67586210	1.00[ASN][1000 genomes]
rs6946420	0.92[CEU][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6962037	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6970145	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7782453	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799818	0.92[CEU][hapmap];1.00[ASN][1000 genomes]
rs7803989	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7811152	0.85[CEU][hapmap];0.85[YRI][hapmap];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831153	chr7:138078179-138265648	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv1030956	chr7:138163169-138579519	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138147200-138183800	Weak transcription	Primary B cells from cord blood	blood
2	chr7:138147200-138189000	Weak transcription	Thymus	Thymus
3	chr7:138149800-138188600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr7:138153800-138184200	Weak transcription	Fetal Stomach	stomach
5	chr7:138155200-138184200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:138157600-138191400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:138160600-138182200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:138161800-138195800	Weak transcription	Fetal Brain Female	brain
9	chr7:138163600-138183400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr7:138163600-138184000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr7:138163600-138184200	Weak transcription	Aorta	Aorta
12	chr7:138163600-138184200	Weak transcription	Fetal Thymus	thymus
13	chr7:138164000-138191400	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr7:138164000-138199800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:138164400-138184200	Weak transcription	Ovary	ovary
16	chr7:138165000-138192000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:138165600-138184000	Weak transcription	Primary T cells from cord blood	blood
18	chr7:138166600-138184000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:138168000-138181400	Weak transcription	Fetal Intestine Small	intestine
20	chr7:138168000-138196200	Weak transcription	Left Ventricle	heart
21	chr7:138168800-138184200	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr7:138169000-138190200	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr7:138172800-138184400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr7:138173800-138183400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr7:138174600-138184200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr7:138175200-138201200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr7:138175400-138185200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr7:138175800-138183000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr7:138176000-138183400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr7:138176200-138184000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr7:138176200-138184000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr7:138176200-138184000	Weak transcription	Dnd41	blood
33	chr7:138176400-138186800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr7:138176600-138183800	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr7:138176600-138184000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr7:138176600-138184000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr7:138176600-138190200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr7:138176600-138203600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr7:138176800-138184000	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr7:138177000-138184200	Weak transcription	Gastric	stomach
41	chr7:138177000-138184200	Weak transcription	Lung	lung
42	chr7:138177000-138189800	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr7:138177000-138190200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:138177000-138212600	Weak transcription	Pancreas	Pancrea
45	chr7:138177200-138184000	Weak transcription	Primary B cells from peripheral blood	blood
46	chr7:138177600-138181000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:138177600-138183200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr7:138177600-138183400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:138177600-138194600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:138178200-138180600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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