Variant report

Variant	rs697221
Chromosome Location	chr12:57911160-57911161
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:93)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:93 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:57911067-57911379	ECC-1	luminal epithelium:	n/a	n/a
2	JUND	chr12:57909651-57911445	HCT-116	colon:	n/a	chr12:57910968-57910977
3	JUND	chr12:57908393-57911701	HCT-116	colon:	n/a	chr12:57910968-57910977
4	POLR2A	chr12:57908101-57916508	PANC-1	pancreas:	n/a	n/a
5	POLR2A	chr12:57907839-57915181	PFSK-1	brain:	n/a	n/a
6	POLR2A	chr12:57908478-57911630	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr12:57908399-57911468	GM12878	blood:	n/a	n/a
8	FOS	chr12:57911047-57911299	MCF10A-Er-Src	breast:	n/a	n/a
9	POLR2A	chr12:57908140-57911521	SK-N-MC	brain:	n/a	n/a
10	POLR2A	chr12:57908340-57911670	GM12891	blood:	n/a	n/a
11	POLR2A	chr12:57910971-57911456	MCF-7	breast:	n/a	n/a
12	HEY1	chr12:57909567-57914433	K562	blood:	n/a	n/a
13	POLR2A	chr12:57908219-57914828	A549	lung:	n/a	n/a
14	POLR2A	chr12:57904506-57914962	K562	blood:	n/a	n/a
15	POLR2A	chr12:57910709-57911344	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr12:57908236-57914960	HepG2	liver:	n/a	n/a
17	CHD2	chr12:57911154-57911265	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr12:57908014-57914558	U87	brain:	n/a	n/a
19	TEAD4	chr12:57909107-57911603	K562	blood:	n/a	n/a
20	POLR2A	chr12:57911052-57911303	GM12878	blood:	n/a	n/a
21	GTF2F1	chr12:57911110-57911379	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr12:57908255-57914954	IMR90	lung:	n/a	n/a
23	USF2	chr12:57908203-57911431	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr12:57908390-57911582	K562	blood:	n/a	n/a
25	POLR2A	chr12:57910806-57911390	GM12891	blood:	n/a	n/a
26	POLR2A	chr12:57908093-57915086	PANC-1	pancreas:	n/a	n/a
27	POLR2A	chr12:57908382-57921207	K562	blood:	n/a	n/a
28	FOS	chr12:57911068-57911268	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr12:57908268-57914527	GM12878	blood:	n/a	n/a
30	TRIM28	chr12:57909262-57911532	K562	blood:	n/a	n/a
31	TEAD4	chr12:57908193-57911650	K562	blood:	n/a	n/a
32	POLR2A	chr12:57910417-57911433	HL-60	blood:	n/a	n/a
33	TBL1XR1	chr12:57909273-57911448	K562	blood:	n/a	n/a
34	POLR2A	chr12:57909681-57911540	GM18505	blood:	n/a	n/a
35	POLR2A	chr12:57911072-57911338	SK-N-SH	brain:	n/a	n/a
36	POLR2A	chr12:57908090-57915139	K562	blood:	n/a	n/a
37	POLR2A	chr12:57911027-57911414	MCF10A-Er-Src	breast:	n/a	n/a
38	SMC3	chr12:57910986-57911379	Hela-S3	cervix:	n/a	n/a
39	HEY1	chr12:57908353-57911297	HepG2	liver:	n/a	n/a
40	POLR2A	chr12:57911049-57911377	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr12:57908603-57912530	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr12:57908180-57911486	GM12891	blood:	n/a	n/a
43	POLR2A	chr12:57908632-57911434	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr12:57908195-57911683	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr12:57908850-57911500	HepG2	liver:	n/a	n/a
46	POLR2A	chr12:57908443-57911694	HepG2	liver:	n/a	n/a
47	ZMIZ1	chr12:57908460-57911396	K562	blood:	n/a	n/a
48	POLR2A	chr12:57911083-57911301	A549	lung:	n/a	n/a
49	FOS	chr12:57911030-57911312	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr12:57908424-57912495	K562	blood:	n/a	n/a

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57879207..57888227-chr12:57906247..57918451,36	K562	blood:
2	chr12:57849885..57859254-chr12:57908711..57915821,16	K562	blood:
3	chr12:57909973..57915898-chr12:58127755..58134567,15	K562	blood:
4	chr12:57910924..57913637-chr12:58087334..58089189,3	K562	blood:
5	chr12:57908910..57916122-chr12:58022622..58031573,17	K562	blood:
6	chr12:57909425..57911920-chr12:57994928..57996477,2	K562	blood:
7	chr12:57850154..57858218-chr12:57910899..57919538,20	K562	blood:
8	chr12:57909291..57914221-chr12:58144639..58148673,6	K562	blood:
9	chr12:57909761..57911469-chr6:25966764..25969575,2	K562	blood:
10	chr12:57910612..57912523-chr12:58153055..58155888,2	K562	blood:
11	chr12:57889487..57901620-chr12:57907600..57919310,30	K562	blood:
12	chr12:57892733..57897365-chr12:57908296..57912099,4	MCF-7	breast:
13	chr12:57880356..57884964-chr12:57910434..57915758,10	MCF-7	breast:
14	chr12:57879869..57888452-chr12:57905809..57918310,36	K562	blood:
15	chr12:57881044..57886958-chr12:57910925..57918058,16	MCF-7	breast:
16	chr12:57908910..57916403-chr12:58022622..58028885,15	K562	blood:
17	chr12:57909956..57912484-chr19:1273775..1275883,2	K562	blood:
18	chr12:57909076..57912703-chr12:58030683..58034118,3	K562	blood:

No data

Variant related genes	Relation type
MBD6	TF binding region
ENSG00000111087	Chromatin interaction
ENSG00000166986	Chromatin interaction
ENSG00000135506	Chromatin interaction
ENSG00000135454	Chromatin interaction
ENSG00000123329	Chromatin interaction
ENSG00000135446	Chromatin interaction
ENSG00000135439	Chromatin interaction
ENSG00000228300	Chromatin interaction
ENSG00000135452	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1148552	0.80[LWK][hapmap];0.97[MKK][hapmap]
rs1148553	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1148554	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148555	0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148557	0.92[ASW][hapmap];0.92[CEU][hapmap];0.81[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1284465	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1284605	0.92[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1284606	0.81[AMR][1000 genomes]
rs1299737	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1629410	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1669294	0.90[EUR][1000 genomes]
rs1669296	0.84[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1669297	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1678537	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.96[TSI][hapmap];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1679368	0.94[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1709871	0.92[ASW][hapmap];0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.96[TSI][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1709874	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2127318	0.92[CEU][hapmap];0.81[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2620677	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2620679	0.92[ASW][hapmap];0.92[CEU][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2672571	0.92[ASW][hapmap];0.85[CEU][hapmap];0.92[CHD][hapmap];0.95[GIH][hapmap];0.91[MEX][hapmap];0.96[TSI][hapmap]
rs2928382	0.88[EUR][1000 genomes]
rs2943696	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3782129	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3847699	0.92[CEU][hapmap];0.81[CHB][hapmap];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs474544	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4760273	0.85[EUR][1000 genomes]
rs496245	0.85[CEU][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs508904	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs511752	0.85[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes]
rs542278	0.84[CHB][hapmap];0.92[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.96[TSI][hapmap]
rs703835	0.92[ASW][hapmap];0.92[CEU][hapmap];0.81[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs703836	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs703837	0.92[ASW][hapmap];0.92[CEU][hapmap];0.81[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs703838	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs703839	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7299631	0.94[EUR][1000 genomes]
rs747340	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs775236	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs775237	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs775241	0.92[ASW][hapmap];0.92[CEU][hapmap];0.81[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs775323	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs775324	0.92[ASW][hapmap];0.92[CEU][hapmap];0.80[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs776038	1.00[ASW][hapmap];0.85[CEU][hapmap];0.92[CHD][hapmap];0.95[GIH][hapmap];0.91[MEX][hapmap];0.96[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs776039	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7964074	0.92[CEU][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes]
rs796546	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7969683	0.84[EUR][1000 genomes]
rs899653	0.92[CHD][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap]
rs9737891	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899117	chr12:57811414-57926472	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers 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	103 gene(s)	inside rSNPs	diseases
2	nsv899118	chr12:57811414-57946477	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases
3	esv1812398	chr12:57829733-58001868	Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758310	chr12:57829733-58001868	Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS 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	96 gene(s)	inside rSNPs	diseases
5	esv2759901	chr12:57829733-58001868	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv428283	chr12:57829733-58001868	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
7	nsv469411	chr12:57844049-57921188	Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
8	nsv559032	chr12:57844049-57921188	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
9	nsv559033	chr12:57848639-57946477	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
10	nsv899119	chr12:57851182-57923451	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
11	nsv559034	chr12:57859932-58012233	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
12	nsv1038741	chr12:57877355-58174506	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer 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 miRNA target site	126 gene(s)	inside rSNPs	diseases
13	nsv541503	chr12:57877355-58174506	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
14	nsv899120	chr12:57886609-57921188	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS 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	72 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs697221	KRT7	cis	cerebellum	SCAN
rs697221	AVIL	cis	cerebellum	SCAN
rs697221	ACVRL1	cis	cerebellum	SCAN
rs697221	SERPINB1	trans	lymphoblastoid	seeQTL
rs697221	CALCOCO1	cis	cerebellum	SCAN
rs697221	ATF7	cis	cerebellum	SCAN
rs697221	ITGB7	cis	cerebellum	SCAN
rs697221	STAT6	cis	parietal	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57883200-57911200	Strong transcription	Fetal Intestine Small	intestine
2	chr12:57885600-57911200	Weak transcription	Fetal Heart	heart
3	chr12:57888600-57912200	Strong transcription	Fetal Stomach	stomach
4	chr12:57900600-57912000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr12:57900600-57912800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr12:57901600-57911800	Strong transcription	Lung	lung
7	chr12:57901800-57911600	Strong transcription	Thymus	Thymus
8	chr12:57901800-57911800	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr12:57901800-57911800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr12:57902000-57912400	Strong transcription	H1 Cell Line	embryonic stem cell
11	chr12:57902200-57911600	Strong transcription	Fetal Muscle Leg	muscle
12	chr12:57902200-57912000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:57902200-57912000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr12:57902200-57912400	Strong transcription	H9 Cell Line	embryonic stem cell
15	chr12:57902400-57911200	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr12:57902400-57911600	Strong transcription	Fetal Thymus	thymus
17	chr12:57902400-57911800	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr12:57902400-57911800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr12:57902400-57912000	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr12:57902400-57912000	Strong transcription	Primary B cells from cord blood	blood
21	chr12:57902400-57912000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr12:57902400-57912000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr12:57902400-57912000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr12:57902400-57912200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:57902400-57912200	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr12:57902400-57912400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:57902400-57912800	Strong transcription	Fetal Brain Female	brain
28	chr12:57902600-57911200	Strong transcription	Muscle Satellite Cultured Cells	--
29	chr12:57902600-57911200	Strong transcription	HSMM	muscle
30	chr12:57902600-57911600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr12:57902600-57911800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:57902600-57911800	Strong transcription	HepG2	liver
33	chr12:57902600-57912000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:57902600-57912000	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr12:57902600-57912000	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr12:57902600-57912200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:57902800-57911200	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr12:57902800-57911200	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr12:57902800-57911400	Strong transcription	Fetal Lung	lung
40	chr12:57902800-57911600	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr12:57902800-57912600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr12:57903000-57911200	Strong transcription	Fetal Intestine Large	intestine
43	chr12:57903000-57911200	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr12:57903000-57911600	Strong transcription	Sigmoid Colon	Sigmoid Colon
45	chr12:57903000-57911800	Strong transcription	Primary T cells from cord blood	blood
46	chr12:57903000-57912000	Strong transcription	GM12878-XiMat	blood
47	chr12:57903000-57912200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
48	chr12:57903000-57912200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr12:57903000-57912600	Strong transcription	Brain Germinal Matrix	brain
50	chr12:57903200-57911600	Strong transcription	Fetal Muscle Trunk	muscle

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