Variant report

Variant	rs2799523
Chromosome Location	chr1:92316682-92316683
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	chr1:92309780..92313855-chr1:92314421..92317529,4	K562	blood:

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs1032255	0.88[CEU][hapmap];0.83[JPT][hapmap];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10874980	0.88[JPT][hapmap]
rs11165578	0.83[JPT][hapmap]
rs11576557	1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1192525	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs1192526	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs12094295	0.81[ASN][1000 genomes]
rs1352438	0.88[CEU][hapmap];0.89[JPT][hapmap];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1488692	0.88[CEU][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs1805109	0.86[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1805110	0.86[CEU][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1906586	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2046737	0.88[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2087300	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2129972	0.88[CEU][hapmap];0.89[JPT][hapmap];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2129973	0.88[CEU][hapmap];0.89[JPT][hapmap];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2256471	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2265863	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2391070	0.88[CEU][hapmap];0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2450926	0.88[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2450927	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2489169	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2489170	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2489171	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2489176	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2489178	0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2489184	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2489185	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2489186	0.86[CEU][hapmap];0.88[JPT][hapmap];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2489189	0.86[CEU][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2489192	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634018	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs2634019	0.86[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634020	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634022	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634023	0.85[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634024	0.88[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2634025	0.87[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2634026	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2634027	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2634028	0.86[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2634029	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2634030	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2634032	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2634033	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2634034	0.87[CEU][hapmap];0.89[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2634036	0.88[CEU][hapmap];0.89[JPT][hapmap];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2799512	0.86[CEU][hapmap];0.88[JPT][hapmap];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2799514	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2799515	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2799516	0.88[CEU][hapmap];0.86[JPT][hapmap];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2799517	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2799521	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2799522	0.88[CEU][hapmap];0.89[JPT][hapmap];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2799524	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2799525	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2799526	0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2799528	0.88[YRI][hapmap]
rs2799539	0.89[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2799547	0.88[CEU][hapmap];0.89[JPT][hapmap];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2810903	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs284146	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs284148	0.86[CEU][hapmap];0.88[JPT][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs284150	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs284151	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs284157	0.83[JPT][hapmap]
rs284160	0.86[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs284161	0.88[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs284162	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs284163	0.86[CEU][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs284164	0.86[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3103332	0.88[CEU][hapmap];0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3103333	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs449960	0.87[CEU][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6604062	1.00[YRI][hapmap]
rs717923	0.89[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs901913	0.86[CEU][hapmap];0.88[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs901914	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs901915	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs901917	0.88[CEU][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1005917	chr1:92189945-92378683	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv524845	chr1:92215725-92598705	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv462517	chr1:92215725-92598705	Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv546810	chr1:92215725-92598705	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv1006318	chr1:92216408-92608324	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv432498	chr1:92218245-92618323	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1004570	chr1:92220544-92622129	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv1014837	chr1:92233905-92618839	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv535031	chr1:92233905-92618839	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv1012134	chr1:92235485-92598800	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv546818	chr1:92236048-92579206	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv546819	chr1:92256626-92558583	Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv546820	chr1:92273644-92558583	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
21	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
22	nsv1007270	chr1:92289298-92598800	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
23	nsv1002730	chr1:92302541-92565229	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92296400-92335800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr1:92300800-92329600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:92308200-92317400	Weak transcription	Lung	lung
4	chr1:92312000-92316800	Weak transcription	NH-A	brain
5	chr1:92312000-92316800	Weak transcription	NHEK	skin
6	chr1:92312000-92317000	Weak transcription	Gastric	stomach
7	chr1:92312000-92329800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr1:92312000-92337200	Weak transcription	Fetal Intestine Small	intestine
9	chr1:92312200-92316800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:92312200-92316800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:92312200-92317000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr1:92312200-92317000	Weak transcription	Fetal Intestine Large	intestine
13	chr1:92312600-92316800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:92312600-92319600	Weak transcription	Placenta	Placenta
15	chr1:92312600-92322200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr1:92312800-92325600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr1:92313600-92316800	Weak transcription	Liver	Liver
18	chr1:92313800-92328200	Weak transcription	Esophagus	oesophagus
19	chr1:92314000-92317000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr1:92315000-92316800	Weak transcription	Pancreas	Pancrea
21	chr1:92315000-92329800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr1:92315200-92330200	Weak transcription	Spleen	Spleen
23	chr1:92315800-92316800	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr1:92315800-92318000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr1:92316000-92317200	Enhancers	Colonic Mucosa	Colon
26	chr1:92316000-92317600	Enhancers	Aorta	Aorta
27	chr1:92316000-92318200	Enhancers	Left Ventricle	heart
28	chr1:92316000-92318200	Enhancers	Psoas Muscle	Psoas
29	chr1:92316200-92317600	Enhancers	Stomach Mucosa	stomach
30	chr1:92316400-92316800	Enhancers	Primary T cells fromperipheralblood	blood
31	chr1:92316400-92316800	Weak transcription	Brain Hippocampus Middle	brain
32	chr1:92316400-92316800	Enhancers	Brain Substantia Nigra	brain
33	chr1:92316400-92316800	Enhancers	Duodenum Mucosa	Duodenum
34	chr1:92316400-92317000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr1:92316400-92317000	Flanking Active TSS	Colon Smooth Muscle	Colon
36	chr1:92316400-92317200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:92316400-92317200	Enhancers	Small Intestine	intestine
38	chr1:92316400-92317400	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:92316400-92317400	Enhancers	Fetal Kidney	kidney
40	chr1:92316400-92317400	Flanking Active TSS	Fetal Lung	lung
41	chr1:92316400-92317600	Flanking Active TSS	Stomach Smooth Muscle	stomach
42	chr1:92316400-92317600	Flanking Active TSS	A549	lung
43	chr1:92316400-92317600	Flanking Active TSS	NHLF	lung
44	chr1:92316400-92317800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr1:92316400-92318000	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr1:92316400-92318000	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr1:92316600-92316800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr1:92316600-92316800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:92316600-92316800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr1:92316600-92316800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links