Variant report

Variant	rs2333410
Chromosome Location	chr17:57137129-57137130
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:57095356..57201201-chr17:57905452..57953516,1644	MCF-7	breast:
2	chr17:57113105..57201250-chr17:57905452..57952793,1492	MCF-7	breast:
3	chr17:56735229..56738018-chr17:57136101..57138096,2	MCF-7	breast:
4	chr17:56736378..56737995-chr17:57136674..57139125,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000062716	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000202077	Chromatin interaction

Extended variants
information (count: 84 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10853008	0.81[CEU][hapmap]
rs11079368	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11654986	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.82[EUR][1000 genomes]
rs11656413	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11658694	0.84[EUR][1000 genomes]
rs11868348	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12051897	0.82[GIH][hapmap]
rs12452313	0.88[CEU][hapmap];0.83[CHB][hapmap];0.82[AMR][1000 genomes]
rs12603238	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12936058	0.96[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12938821	0.81[EUR][1000 genomes]
rs12944948	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes]
rs12947785	0.96[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.81[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12948039	0.82[ASN][1000 genomes]
rs12948746	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1588322	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1871751	0.84[EUR][1000 genomes]
rs1967415	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2055779	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2158966	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3826353	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.97[TSI][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4076229	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap]
rs4132925	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap]
rs4372750	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4398153	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap]
rs4500802	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4598970	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4636974	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes]
rs4932693	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56297715	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56360354	0.84[EUR][1000 genomes]
rs57869245	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs58092632	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6416932	1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6416933	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6503887	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6503889	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6503890	0.96[CEU][hapmap];0.95[CHB][hapmap];0.85[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6503893	1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6503894	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6503896	0.83[EUR][1000 genomes]
rs7207693	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7208505	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.84[EUR][1000 genomes]
rs7214098	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.84[EUR][1000 genomes]
rs7214335	0.91[CEU][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7214892	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7215808	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[JPT][hapmap]
rs7216680	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7218105	1.00[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72628394	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7502947	0.87[MEX][hapmap]
rs7503190	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8067264	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8069033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8071280	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8072712	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8076121	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8081297	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8081967	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8082544	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8182277	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9892062	0.91[CEU][hapmap];0.90[CHB][hapmap];0.84[JPT][hapmap];0.81[EUR][1000 genomes]
rs9892795	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9894274	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes]
rs9898916	0.91[CEU][hapmap];0.84[CHB][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9901181	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes]
rs9902994	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap]
rs9911578	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv908643	chr17:56803028-57249010	Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
2	nsv908644	chr17:56803028-57371432	Strong transcription Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
3	esv3335958	chr17:56849544-57385398	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
4	nsv908645	chr17:56857281-57208752	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	150 gene(s)	inside rSNPs	diseases
5	nsv1065063	chr17:56954121-57346694	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers 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 miRNA target site	227 gene(s)	inside rSNPs	diseases
6	nsv1064384	chr17:57049519-57346694	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
7	nsv908646	chr17:57061238-57255810	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking 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	206 gene(s)	inside rSNPs	diseases
8	nsv833499	chr17:57070693-57288410	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers 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	208 gene(s)	inside rSNPs	diseases
9	nsv1066388	chr17:57082013-57339981	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	209 gene(s)	inside rSNPs	diseases
10	esv2758462	chr17:57082579-57425634	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	213 gene(s)	inside rSNPs	diseases
11	esv2758699	chr17:57082579-57425634	Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	213 gene(s)	inside rSNPs	diseases
12	nsv1066467	chr17:57117682-57338731	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	200 gene(s)	inside rSNPs	diseases
13	nsv1057209	chr17:57117682-57742240	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	240 gene(s)	inside rSNPs	diseases
14	nsv543396	chr17:57117682-57742240	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers 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 miRNA target site	240 gene(s)	inside rSNPs	diseases
15	nsv1066788	chr17:57126446-57344129	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	193 gene(s)	inside rSNPs	diseases
16	nsv482858	chr17:57136446-57288615	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS 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	184 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2333410	TRIM37	cis	Adipose Subcutaneous	GTEx
rs2333410	RAD51C	Cis_1M	lymphoblastoid	RTeQTL
rs2333410	TRIM37	cis	Muscle Skeletal	GTEx
rs2333410	TRIM37	cis	Whole Blood	GTEx

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:57055800-57153600	Weak transcription	Aorta	Aorta
2	chr17:57066000-57151400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr17:57073200-57143800	Weak transcription	Fetal Brain Male	brain
4	chr17:57079800-57167000	Weak transcription	Small Intestine	intestine
5	chr17:57104200-57159600	Weak transcription	Psoas Muscle	Psoas
6	chr17:57105200-57139600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr17:57106200-57170400	Weak transcription	NHLF	lung
8	chr17:57112400-57143800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr17:57112800-57158800	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr17:57113000-57158000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr17:57113400-57142600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr17:57114800-57141800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr17:57115000-57142400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr17:57115000-57159000	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr17:57115400-57142800	Strong transcription	HUES6 Cell Line	embryonic stem cell
16	chr17:57121000-57147000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr17:57121200-57156800	Weak transcription	Brain Angular Gyrus	brain
18	chr17:57121400-57183400	Weak transcription	Gastric	stomach
19	chr17:57121600-57166200	Weak transcription	Esophagus	oesophagus
20	chr17:57121800-57166400	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr17:57121800-57181800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr17:57122000-57156000	Weak transcription	Colonic Mucosa	Colon
23	chr17:57122400-57137200	Weak transcription	Brain Hippocampus Middle	brain
24	chr17:57123800-57145200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr17:57124800-57167600	Strong transcription	Dnd41	blood
26	chr17:57125800-57148400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr17:57126000-57147000	Weak transcription	Brain Substantia Nigra	brain
28	chr17:57126800-57139600	Weak transcription	HSMM	muscle
29	chr17:57126800-57143200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr17:57127000-57166400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr17:57127000-57181800	Weak transcription	Brain Cingulate Gyrus	brain
32	chr17:57127200-57137200	Weak transcription	HMEC	breast
33	chr17:57127200-57167000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr17:57127800-57145000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr17:57128000-57139400	Weak transcription	HepG2	liver
36	chr17:57128000-57156000	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr17:57128200-57147000	Weak transcription	Fetal Kidney	kidney
38	chr17:57129600-57146800	Weak transcription	Primary hematopoietic stem cells	blood
39	chr17:57129800-57142600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr17:57130000-57137600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr17:57130600-57143600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr17:57130600-57159200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr17:57130800-57142400	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr17:57131200-57138000	Strong transcription	Primary T cells from cord blood	blood
45	chr17:57131200-57138200	Strong transcription	H1 Cell Line	embryonic stem cell
46	chr17:57131600-57137600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr17:57131800-57137600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr17:57131800-57137600	Strong transcription	Fetal Stomach	stomach
49	chr17:57131800-57137800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr17:57132000-57137600	Strong transcription	Fetal Intestine Small	intestine

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