Variant report

Variant	rs3097731
Chromosome Location	chr10:355430-355431
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:354319..356536-chr10:361569..363521,3	MCF-7	breast:

Extended variants
information (count: 109 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10736974	1.00[AMR][1000 genomes]
rs10736988	1.00[MEX][hapmap]
rs10751932	1.00[AMR][1000 genomes]
rs10751936	1.00[AMR][1000 genomes]
rs10795023	1.00[AMR][1000 genomes]
rs10795053	1.00[AMR][1000 genomes]
rs12773603	1.00[AMR][1000 genomes]
rs12784967	1.00[AMR][1000 genomes]
rs17159564	1.00[MEX][hapmap]
rs3097718	1.00[MEX][hapmap];0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs3097721	1.00[MEX][hapmap]
rs3097722	1.00[AMR][1000 genomes]
rs3097723	1.00[AMR][1000 genomes]
rs3097725	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs3097726	0.82[AFR][1000 genomes]
rs3097727	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3097728	1.00[YRI][hapmap]
rs3123227	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs3123231	1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs3123233	1.00[AMR][1000 genomes]
rs3123237	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs3123243	1.00[AMR][1000 genomes]
rs3123253	0.86[AFR][1000 genomes]
rs3125026	0.87[MKK][hapmap]
rs3125032	1.00[AMR][1000 genomes]
rs3125035	1.00[LWK][hapmap];0.93[MKK][hapmap];0.82[YRI][hapmap];0.91[AFR][1000 genomes]
rs3125036	0.82[YRI][hapmap];0.86[AFR][1000 genomes]
rs3125039	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3131996	1.00[MEX][hapmap]
rs3132000	1.00[AMR][1000 genomes]
rs3132005	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs3132007	1.00[AMR][1000 genomes]
rs3132009	0.82[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3132010	0.82[YRI][hapmap]
rs4242753	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs4242754	1.00[AMR][1000 genomes]
rs4242759	1.00[MEX][hapmap]
rs4332447	1.00[AMR][1000 genomes]
rs4366415	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs4880609	1.00[AMR][1000 genomes]
rs4880610	1.00[MEX][hapmap];0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs4880618	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs4880624	1.00[MEX][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs4880654	1.00[AMR][1000 genomes]
rs4881200	1.00[MEX][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs4881290	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs61683125	1.00[AMR][1000 genomes]
rs6560837	1.00[MEX][hapmap]
rs6560839	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs7068944	1.00[MEX][hapmap];0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs7071457	1.00[AMR][1000 genomes]
rs7073298	1.00[AMR][1000 genomes]
rs7080493	1.00[AMR][1000 genomes]
rs7087181	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs7088111	1.00[AMR][1000 genomes]
rs7090704	1.00[MEX][hapmap]
rs7091570	1.00[AMR][1000 genomes]
rs7091790	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs7095303	1.00[AMR][1000 genomes]
rs7096386	1.00[AMR][1000 genomes]
rs73581728	1.00[AMR][1000 genomes]
rs73583756	1.00[AMR][1000 genomes]
rs7898532	1.00[AMR][1000 genomes]
rs816589	1.00[MEX][hapmap]
rs816590	1.00[MEX][hapmap]
rs816601	1.00[MEX][hapmap]
rs9731043	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:42 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531919	chr10:60001-668649	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv817282	chr10:224406-358626	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv1041536	chr10:224406-370879	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv540389	chr10:224406-370879	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv949174	chr10:224406-437940	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv1046703	chr10:224406-461742	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv540380	chr10:224406-461742	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv817534	chr10:224406-503460	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv1045404	chr10:224406-520269	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
10	nsv1042404	chr10:224406-567104	Genic enhancers Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer 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	9 gene(s)	inside rSNPs	diseases
11	nsv540381	chr10:224406-567104	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
12	nsv1046313	chr10:224406-691123	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv540385	chr10:224406-691123	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
14	nsv1036501	chr10:224406-775824	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
15	nsv1052660	chr10:224406-785929	Weak transcription Enhancers Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
16	nsv1043752	chr10:224406-789665	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
17	nsv916363	chr10:224406-816628	ZNF genes & repeats Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
18	nsv916591	chr10:224406-1088734	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
19	nsv540386	chr10:224406-1197416	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
20	nsv1039358	chr10:225071-406871	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
21	nsv540390	chr10:225071-406871	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
22	nsv530114	chr10:226083-596534	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
23	nsv1037147	chr10:248463-461742	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
24	nsv540391	chr10:248463-461742	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
25	nsv1035580	chr10:248463-832240	Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
26	nsv540392	chr10:248463-832240	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
27	nsv491747	chr10:248464-451013	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
28	nsv1038164	chr10:248529-456953	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
29	nsv540393	chr10:248529-456953	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
30	nsv466693	chr10:255222-566195	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
31	nsv549750	chr10:255222-566195	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
32	nsv894696	chr10:260544-368295	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
33	nsv894697	chr10:260544-387060	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
34	nsv894698	chr10:273344-387060	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS 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 miRNA target site	6 gene(s)	inside rSNPs	diseases
35	nsv1040466	chr10:278544-626866	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
36	nsv932647	chr10:278852-624284	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
37	nsv530115	chr10:294172-633529	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
38	nsv1047760	chr10:297839-362082	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
39	nsv540394	chr10:297839-362082	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
40	nsv894699	chr10:313304-487973	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
41	nsv549751	chr10:313304-734229	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers 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 miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
42	nsv894700	chr10:338553-487973	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:321400-360400	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr10:326000-363800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr10:327800-360800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr10:329000-375200	Weak transcription	Psoas Muscle	Psoas
5	chr10:329200-357800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr10:329200-360400	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr10:330400-359000	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr10:331400-375400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr10:333000-362600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr10:337400-363200	Weak transcription	Esophagus	oesophagus
11	chr10:342400-375600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr10:343600-363200	Weak transcription	Fetal Brain Male	brain
13	chr10:343600-363600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr10:343800-358200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr10:344200-369400	Weak transcription	A549	lung
16	chr10:344200-369600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr10:344400-360400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr10:344400-363200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr10:344800-360400	Weak transcription	Small Intestine	intestine
20	chr10:346000-367400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr10:346400-356600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr10:347000-356600	Strong transcription	Brain Inferior Temporal Lobe	brain
23	chr10:349200-379400	Weak transcription	Thymus	Thymus
24	chr10:350200-358400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr10:350200-358400	Strong transcription	Stomach Smooth Muscle	stomach
26	chr10:350600-356000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr10:351200-360000	Weak transcription	Primary T cells from cord blood	blood
28	chr10:351200-363200	Weak transcription	Aorta	Aorta
29	chr10:351400-367600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr10:351600-356600	Genic enhancers	Fetal Muscle Leg	muscle
31	chr10:351600-358400	Strong transcription	Fetal Stomach	stomach
32	chr10:352000-355600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr10:352000-357200	Genic enhancers	Adipose Nuclei	Adipose
34	chr10:352000-358400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr10:352200-356000	Strong transcription	Brain Substantia Nigra	brain
36	chr10:352200-357000	Strong transcription	Brain Hippocampus Middle	brain
37	chr10:352200-358600	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr10:352200-358600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr10:352600-358000	Strong transcription	Brain Germinal Matrix	brain
40	chr10:352800-358200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr10:353000-355600	Strong transcription	Fetal Brain Female	brain
42	chr10:353200-355800	Strong transcription	NHLF	lung
43	chr10:353200-357600	Enhancers	Primary B cells from cord blood	blood
44	chr10:353200-375600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr10:353200-375600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr10:353400-357600	Enhancers	Primary B cells from peripheral blood	blood
47	chr10:353400-363200	Weak transcription	Fetal Kidney	kidney
48	chr10:353400-367000	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr10:353600-355600	Strong transcription	Right Ventricle	heart
50	chr10:353600-363000	Weak transcription	Fetal Heart	heart

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