Variant report

Variant	rs10773003
Chromosome Location	chr12:123775127-123775128
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:123775064-123775170	K562	blood:	n/a	n/a
2	POLR2A	chr12:123774931-123775246	K562	blood:	n/a	n/a
3	POLR2A	chr12:123774964-123775329	K562	blood:	n/a	n/a
4	POLR2A	chr12:123774956-123775234	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:123753970..123756474-chr12:123774953..123777453,3	K562	blood:
2	chr12:123716096..123717639-chr12:123774721..123776703,2	K562	blood:
3	chr12:123775006..123777510-chr12:123810415..123813403,2	K562	blood:

Variant related genes	Relation type
ENSG00000270113	TF binding region
ENSG00000111328	Chromatin interaction
ENSG00000130921	Chromatin interaction

Extended variants
information (count: 183 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:177)

rs_ID	r²[population]
rs10082867	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10444439	0.95[CHB][hapmap];0.94[JPT][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10444449	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10744151	0.80[JPT][hapmap]
rs10744152	0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs10744153	0.80[ASN][1000 genomes]
rs10744154	0.80[ASN][1000 genomes]
rs10772997	0.84[JPT][hapmap]
rs10773000	0.94[JPT][hapmap]
rs10773004	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10773005	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.93[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10773006	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10773007	0.82[GIH][hapmap];1.00[YRI][hapmap]
rs10773014	1.00[YRI][hapmap]
rs10846489	0.86[CHD][hapmap];0.94[JPT][hapmap]
rs10846497	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10846505	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10846506	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10846509	0.82[GIH][hapmap];1.00[YRI][hapmap]
rs10846510	1.00[YRI][hapmap]
rs10846514	0.82[GIH][hapmap];1.00[YRI][hapmap]
rs10846517	0.82[CHB][hapmap];0.94[CHD][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs10846518	0.82[GIH][hapmap];1.00[YRI][hapmap]
rs10846519	0.94[CHD][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs10846523	0.94[CHD][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs11057223	1.00[CEU][hapmap];0.86[CHD][hapmap];0.94[GIH][hapmap];0.94[JPT][hapmap];0.86[TSI][hapmap];1.00[YRI][hapmap]
rs11057238	0.89[ASN][1000 genomes]
rs11057240	1.00[YRI][hapmap]
rs11057242	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11057248	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11057250	1.00[YRI][hapmap]
rs11057251	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11057254	0.96[ASN][1000 genomes]
rs11057261	0.96[ASN][1000 genomes]
rs11057266	0.82[GIH][hapmap];1.00[YRI][hapmap]
rs11057273	1.00[CEU][hapmap];0.90[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11057275	0.93[ASN][1000 genomes]
rs11057276	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11057283	0.80[ASN][1000 genomes]
rs11057284	0.96[ASN][1000 genomes]
rs11057287	0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs1109559	0.86[CHD][hapmap];0.94[JPT][hapmap]
rs1109560	1.00[CEU][hapmap];0.94[JPT][hapmap]
rs11503021	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11608297	0.85[ASN][1000 genomes]
rs11608305	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11611141	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11611677	0.93[ASN][1000 genomes]
rs11611679	0.91[ASN][1000 genomes]
rs11611680	0.92[ASN][1000 genomes]
rs11611694	0.91[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11612234	0.80[ASN][1000 genomes]
rs12317103	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12317452	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12366872	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12367421	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12371973	1.00[YRI][hapmap]
rs12582153	0.99[ASN][1000 genomes]
rs13303208	0.89[ASN][1000 genomes]
rs1402275	0.85[YRI][hapmap]
rs1568428	0.94[JPT][hapmap]
rs1615350	0.84[JPT][hapmap]
rs1727293	0.90[JPT][hapmap]
rs1727295	0.84[JPT][hapmap]
rs1727301	0.85[JPT][hapmap]
rs1727302	0.84[JPT][hapmap]
rs1727307	0.80[JPT][hapmap]
rs1790094	0.80[JPT][hapmap]
rs1790104	0.85[JPT][hapmap]
rs1790106	0.80[JPT][hapmap]
rs1790121	0.80[JPT][hapmap]
rs1879379	0.94[JPT][hapmap]
rs2271976	1.00[CEU][hapmap];0.94[JPT][hapmap]
rs2682427	0.85[JPT][hapmap]
rs28410096	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[ASN][1000 genomes]
rs28414347	0.94[CHD][hapmap];0.84[JPT][hapmap]
rs28418709	0.80[ASN][1000 genomes]
rs28419092	0.96[ASN][1000 genomes]
rs28450974	0.94[ASN][1000 genomes]
rs28461471	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs28475177	0.82[GIH][hapmap];1.00[YRI][hapmap]
rs28496545	0.88[ASN][1000 genomes]
rs28498205	0.94[ASN][1000 genomes]
rs28501453	0.94[CHD][hapmap];0.84[JPT][hapmap]
rs28503862	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs28516750	0.90[ASN][1000 genomes]
rs28517382	0.80[ASN][1000 genomes]
rs28532037	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.94[ASN][1000 genomes]
rs28533432	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs28556815	0.84[ASN][1000 genomes]
rs28565984	0.81[ASN][1000 genomes]
rs28577594	0.89[ASN][1000 genomes]
rs28581850	0.94[ASN][1000 genomes]
rs28587386	0.94[CHD][hapmap];0.84[JPT][hapmap]
rs28592032	0.94[ASN][1000 genomes]
rs28594416	0.80[ASN][1000 genomes]
rs28595660	0.94[CHD][hapmap];0.84[JPT][hapmap]
rs28613486	0.94[CHD][hapmap];0.84[JPT][hapmap]
rs28631104	0.88[ASN][1000 genomes]
rs28631903	0.80[ASN][1000 genomes]
rs28642812	0.89[ASN][1000 genomes]
rs28655516	0.82[GIH][hapmap];1.00[YRI][hapmap]
rs28660993	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs28690326	0.82[ASN][1000 genomes]
rs28759130	0.80[ASN][1000 genomes]
rs28786830	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs28820735	0.94[ASN][1000 genomes]
rs28825193	0.94[ASN][1000 genomes]
rs28866344	0.90[ASN][1000 genomes]
rs3088303	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34032470	0.85[ASN][1000 genomes]
rs35818434	0.94[ASN][1000 genomes]
rs3803001	0.94[CHD][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs3825141	0.94[CHD][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs4759374	0.82[ASN][1000 genomes]
rs4759375	1.00[YRI][hapmap];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4759376	0.80[ASN][1000 genomes]
rs4759377	1.00[ASW][hapmap];0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4759421	0.80[ASN][1000 genomes]
rs56116847	0.95[ASN][1000 genomes]
rs56197170	0.83[ASN][1000 genomes]
rs56309603	0.86[ASN][1000 genomes]
rs57356592	0.82[ASN][1000 genomes]
rs57416942	0.80[ASN][1000 genomes]
rs58537268	0.82[ASN][1000 genomes]
rs58948739	0.82[ASN][1000 genomes]
rs59295450	0.80[ASN][1000 genomes]
rs60755632	0.82[ASN][1000 genomes]
rs60835840	0.93[ASN][1000 genomes]
rs61058270	0.82[ASN][1000 genomes]
rs61388686	0.96[ASN][1000 genomes]
rs61751327	0.80[ASN][1000 genomes]
rs61953412	0.80[ASN][1000 genomes]
rs61955125	0.86[ASN][1000 genomes]
rs6416290	0.83[ASN][1000 genomes]
rs6488869	0.80[ASN][1000 genomes]
rs6488870	0.80[ASN][1000 genomes]
rs6488871	0.80[ASN][1000 genomes]
rs6488872	0.80[ASN][1000 genomes]
rs6488873	0.87[ASN][1000 genomes]
rs7137243	0.80[ASN][1000 genomes]
rs7139321	0.94[JPT][hapmap]
rs7297649	0.94[CHD][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs7298909	0.93[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7301163	0.80[ASN][1000 genomes]
rs7303754	0.84[ASN][1000 genomes]
rs7310756	0.80[ASN][1000 genomes]
rs7311304	0.80[ASN][1000 genomes]
rs7312145	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7315453	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.92[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73216931	0.89[ASN][1000 genomes]
rs73231950	0.99[ASN][1000 genomes]
rs7484644	0.80[ASN][1000 genomes]
rs7485967	0.80[ASN][1000 genomes]
rs7486223	0.80[ASN][1000 genomes]
rs7488340	0.80[ASN][1000 genomes]
rs7488490	0.93[AFR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7952835	0.80[ASN][1000 genomes]
rs7954704	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7955367	0.80[ASN][1000 genomes]
rs7959415	0.94[CHD][hapmap];0.89[JPT][hapmap];0.80[ASN][1000 genomes]
rs7970080	0.80[ASN][1000 genomes]
rs7972811	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7973131	0.80[ASN][1000 genomes]
rs7973878	0.80[ASN][1000 genomes]
rs7974099	0.89[ASN][1000 genomes]
rs7977563	0.80[ASN][1000 genomes]
rs9284166	0.80[ASN][1000 genomes]
rs9300257	0.80[ASN][1000 genomes]
rs949143	0.80[JPT][hapmap]
rs9669169	0.80[ASN][1000 genomes]
rs9669273	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9669295	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9705407	0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9739171	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9739565	0.80[ASN][1000 genomes]
rs9795593	0.94[CHD][hapmap];0.83[JPT][hapmap];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1825473	chr12:123582855-123822503	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv1803368	chr12:123640853-123822503	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS 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	70 gene(s)	inside rSNPs	diseases
3	esv1830566	chr12:123640853-123822503	Flanking Active TSS Strong transcription Enhancers Weak transcription 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 target site	70 gene(s)	inside rSNPs	diseases
4	esv1836043	chr12:123709409-123822503	Weak transcription Flanking Active TSS Strong transcription Enhancers 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 target site	70 gene(s)	inside rSNPs	diseases
5	nsv1038841	chr12:123757305-124087671	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
6	nsv541622	chr12:123757305-124087671	Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10773003	RP11-282O18.3	cis	Whole Blood	GTEx
rs10773003	CDK2AP1	cis	Whole Blood	GTEx

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123757200-123782600	Weak transcription	Right Atrium	heart
2	chr12:123763200-123775800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr12:123766200-123780000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr12:123769800-123778800	Weak transcription	Fetal Kidney	kidney
5	chr12:123770200-123776800	Weak transcription	Spleen	Spleen
6	chr12:123770200-123778400	Weak transcription	Fetal Lung	lung
7	chr12:123771200-123777800	Weak transcription	Psoas Muscle	Psoas
8	chr12:123771400-123777000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:123771400-123777600	Weak transcription	Right Ventricle	heart
10	chr12:123771400-123777800	Weak transcription	Brain Angular Gyrus	brain
11	chr12:123771600-123776800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr12:123771600-123799800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr12:123771800-123776600	Weak transcription	NHLF	lung
14	chr12:123771800-123777000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr12:123771800-123777200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr12:123771800-123777600	Weak transcription	Esophagus	oesophagus
17	chr12:123771800-123777800	Weak transcription	Ovary	ovary
18	chr12:123771800-123779800	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr12:123771800-123790800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr12:123772000-123776400	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr12:123772000-123776600	Weak transcription	Gastric	stomach
22	chr12:123772000-123777000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr12:123772000-123777400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr12:123772000-123778200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr12:123772200-123775600	Strong transcription	Fetal Intestine Small	intestine
26	chr12:123772200-123776600	Weak transcription	Brain Hippocampus Middle	brain
27	chr12:123772200-123782000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr12:123772400-123775200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:123772400-123777000	Weak transcription	HMEC	breast
30	chr12:123772400-123799800	Strong transcription	Fetal Stomach	stomach
31	chr12:123772400-123847800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr12:123772600-123776600	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr12:123772800-123775400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr12:123772800-123775600	Weak transcription	HSMM	muscle
35	chr12:123772800-123776400	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr12:123772800-123777800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr12:123772800-123789400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr12:123772800-123821000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr12:123773000-123777000	Weak transcription	Colonic Mucosa	Colon
40	chr12:123773000-123777000	Weak transcription	NHDF-Ad	bronchial
41	chr12:123773000-123835200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:123773200-123775400	Weak transcription	Hela-S3	cervix
43	chr12:123773200-123778200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr12:123773200-123778200	Strong transcription	A549	lung
45	chr12:123773200-123785000	Strong transcription	Primary T cells from cord blood	blood
46	chr12:123773200-123830600	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr12:123773200-123834200	Strong transcription	HUES64 Cell Line	embryonic stem cell
48	chr12:123773200-123835000	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr12:123773200-123835000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr12:123773200-123838000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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