Variant report

Variant	rs3827303
Chromosome Location	chr22:22191575-22191576
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:22186046..22188555-chr22:22189974..22192124,2	MCF-7	breast:
2	chr22:22035151..22037450-chr22:22190171..22191825,2	K562	blood:

Extended variants
information (count: 108 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs11089745	0.86[EUR][1000 genomes]
rs1123393	1.00[AFR][1000 genomes]
rs11703249	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[AFR][1000 genomes]
rs11703350	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11703452	1.00[AFR][1000 genomes]
rs11703481	1.00[AFR][1000 genomes]
rs11703624	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11703767	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11704178	1.00[AFR][1000 genomes]
rs11704184	1.00[AFR][1000 genomes]
rs11704248	1.00[AFR][1000 genomes]
rs11704265	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11704433	0.86[EUR][1000 genomes]
rs11704597	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12172215	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12172360	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13054366	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs13058633	0.86[EUR][1000 genomes]
rs13515	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs2070506	1.00[AFR][1000 genomes]
rs2070507	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[AFR][1000 genomes]
rs2073415	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[AFR][1000 genomes]
rs2083564	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[AFR][1000 genomes]
rs2266968	1.00[CEU][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2266974	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[AFR][1000 genomes]
rs2276005	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs2276006	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs2283795	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2283796	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2298434	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4820146	0.86[EUR][1000 genomes]
rs4821263	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs4821336	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4821367	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4821369	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4821371	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4821401	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5749769	0.82[EUR][1000 genomes]
rs5749779	0.94[CHB][hapmap];0.86[EUR][1000 genomes]
rs5749792	0.86[EUR][1000 genomes]
rs5749811	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs5749939	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5749984	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs5750275	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[AFR][1000 genomes]
rs5750281	1.00[AFR][1000 genomes]
rs5750301	1.00[CEU][hapmap];0.87[CHB][hapmap]
rs5754916	0.86[EUR][1000 genomes]
rs5754927	0.93[CHB][hapmap];0.82[EUR][1000 genomes]
rs5754932	1.00[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap]
rs5754944	0.86[EUR][1000 genomes]
rs5754947	1.00[CEU][hapmap];0.88[CHB][hapmap];0.86[EUR][1000 genomes]
rs5754968	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5754970	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5755008	0.86[EUR][1000 genomes]
rs5755040	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs5755074	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs5755579	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs5755745	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5755875	0.91[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs5755884	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs5755978	1.00[CEU][hapmap];0.88[CHB][hapmap];0.85[JPT][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs5755996	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs5756051	1.00[AFR][1000 genomes]
rs5756076	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs5756253	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[AFR][1000 genomes]
rs5756326	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[AFR][1000 genomes]
rs71314794	0.82[EUR][1000 genomes]
rs9607274	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9607286	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9607348	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9607363	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9607370	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9607385	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[AFR][1000 genomes]
rs9607399	1.00[AFR][1000 genomes]
rs9610199	0.82[EUR][1000 genomes]
rs9610219	1.00[CEU][hapmap];0.94[CHB][hapmap];0.86[EUR][1000 genomes]
rs9610228	0.86[EUR][1000 genomes]
rs9610355	1.00[CEU][hapmap];0.93[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9610518	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9610536	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9610574	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9610627	1.00[AFR][1000 genomes]
rs9610702	1.00[AFR][1000 genomes]
rs9610720	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948603	chr22:21928916-22601814	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	422 gene(s)	inside rSNPs	diseases
2	nsv948902	chr22:21928916-22657900	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	426 gene(s)	inside rSNPs	diseases
3	nsv1063962	chr22:21939722-22934593	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	477 gene(s)	inside rSNPs	diseases
4	nsv1058617	chr22:21939922-22934454	Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	477 gene(s)	inside rSNPs	diseases
5	nsv529694	chr22:21957411-22905068	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats 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	474 gene(s)	inside rSNPs	diseases
6	nsv531797	chr22:21977700-22959729	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	476 gene(s)	inside rSNPs	diseases
7	nsv1066403	chr22:22010822-22352262	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats 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	51 gene(s)	inside rSNPs	diseases
8	nsv1066964	chr22:22055123-22228745	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv544604	chr22:22055123-22228745	Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv948580	chr22:22100718-22839559	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers 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	97 gene(s)	inside rSNPs	diseases
11	esv1795495	chr22:22131125-22204916	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv914470	chr22:22131125-22272737	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
13	nsv1059265	chr22:22131125-22457154	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	esv3379268	chr22:22135347-22446281	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
15	esv3385441	chr22:22135777-22320294	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	esv2752404	chr22:22141825-22570417	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
17	esv2422277	chr22:22144108-22442159	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
18	esv2422295	chr22:22144108-22442159	Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
19	esv2422374	chr22:22152248-22595246	Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
20	esv2422403	chr22:22152248-23112582	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
21	nsv1062641	chr22:22157661-22367697	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers 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	39 gene(s)	inside rSNPs	diseases
22	esv2422390	chr22:22157964-23112582	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers 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 miRNA target site	145 gene(s)	inside rSNPs	diseases
23	nsv914471	chr22:22165557-22272737	Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription 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	17 gene(s)	inside rSNPs	diseases
24	esv2763701	chr22:22173533-22573987	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:22174000-22191800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr22:22174600-22191800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr22:22179600-22191600	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr22:22182600-22210400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr22:22185400-22200400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr22:22186800-22191600	Weak transcription	Fetal Intestine Large	intestine
7	chr22:22187000-22191600	Weak transcription	Fetal Brain Male	brain
8	chr22:22187000-22191800	Weak transcription	Fetal Brain Female	brain
9	chr22:22187000-22195000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr22:22187200-22191600	Weak transcription	Liver	Liver
11	chr22:22187200-22191600	Weak transcription	Fetal Intestine Small	intestine
12	chr22:22187200-22191600	Weak transcription	Hela-S3	cervix
13	chr22:22187200-22191800	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr22:22187200-22198200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr22:22187200-22198400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr22:22187200-22200200	Weak transcription	Spleen	Spleen
17	chr22:22187400-22191600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr22:22187400-22191600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr22:22187400-22191600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr22:22187400-22191600	Weak transcription	A549	lung
21	chr22:22187600-22191800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr22:22187600-22191800	Weak transcription	HSMMtube	muscle
23	chr22:22187800-22211000	Weak transcription	Dnd41	blood
24	chr22:22189000-22191600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr22:22189000-22191600	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr22:22189000-22191800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr22:22189000-22192200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr22:22189000-22192200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr22:22189000-22192200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr22:22189000-22192200	Enhancers	K562	blood
31	chr22:22189000-22193200	Enhancers	Colon Smooth Muscle	Colon
32	chr22:22189200-22192400	Enhancers	Adipose Nuclei	Adipose
33	chr22:22189200-22193200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr22:22189200-22193200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr22:22189200-22196000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr22:22189600-22191600	Weak transcription	Primary hematopoietic stem cells	blood
37	chr22:22189600-22191600	Weak transcription	Placenta	Placenta
38	chr22:22189600-22191600	Weak transcription	Gastric	stomach
39	chr22:22189600-22191800	Weak transcription	Left Ventricle	heart
40	chr22:22189600-22191800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr22:22189600-22197400	Weak transcription	Esophagus	oesophagus
42	chr22:22189600-22198600	Weak transcription	Thymus	Thymus
43	chr22:22189600-22200600	Weak transcription	Ovary	ovary
44	chr22:22189800-22191600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr22:22189800-22191600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr22:22190000-22191800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr22:22190000-22191800	Weak transcription	Right Ventricle	heart
48	chr22:22190000-22197600	Weak transcription	Lung	lung
49	chr22:22190000-22201200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr22:22190200-22191800	Weak transcription	Stomach Smooth Muscle	stomach

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