Variant report

Variant	rs2074540
Chromosome Location	chr12:120636549-120636550
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:81)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:81 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:120636134-120636649	HepG2	liver:	n/a	n/a
2	POLR2A	chr12:120636195-120637300	GM12878	blood:	n/a	n/a
3	POLR2A	chr12:120631371-120639781	PANC-1	pancreas:	n/a	n/a
4	POLR2A	chr12:120636178-120639074	A549	lung:	n/a	n/a
5	POLR2A	chr12:120636252-120638005	GM12878	blood:	n/a	n/a
6	POLR2A	chr12:120632029-120639863	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr12:120636242-120637428	GM19193	blood:	n/a	n/a
8	POLR2A	chr12:120636228-120636649	HepG2	liver:	n/a	n/a
9	POLR2A	chr12:120636195-120639774	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr12:120636127-120639423	ECC-1	luminal epithelium:	n/a	n/a
11	POLR2A	chr12:120636151-120638027	GM12891	blood:	n/a	n/a
12	POLR2A	chr12:120636471-120639372	HL-60	blood:	n/a	n/a
13	POLR2A	chr12:120635673-120639688	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr12:120632203-120639596	K562	blood:	n/a	n/a
15	POLR2A	chr12:120636111-120637525	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr12:120636420-120639604	MCF10A-Er-Src	breast:	n/a	n/a
17	CTCF	chr12:120636500-120636650	A549	lung:	n/a	n/a
18	POLR2A	chr12:120635716-120639431	GM12892	blood:	n/a	n/a
19	EP300	chr12:120636124-120636648	T-47D	breast:	n/a	n/a
20	POLR2A	chr12:120631475-120639779	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr12:120632190-120639605	GM12892	blood:	n/a	n/a
22	POLR2A	chr12:120636042-120639720	PANC-1	pancreas:	n/a	n/a
23	PML	chr12:120636084-120637114	K562	blood:	n/a	n/a
24	POLR2A	chr12:120632031-120639569	GM12892	blood:	n/a	n/a
25	POLR2A	chr12:120636133-120639305	U87	brain:	n/a	n/a
26	HEY1	chr12:120636156-120637525	HepG2	liver:	n/a	n/a
27	POLR2A	chr12:120635672-120639608	GM12891	blood:	n/a	n/a
28	POLR2A	chr12:120636479-120637527	HL-60	blood:	n/a	n/a
29	POLR2A	chr12:120636010-120639485	HUVEC	blood vessel:	n/a	n/a
30	POLR2A	chr12:120635799-120639930	HepG2	liver:	n/a	n/a
31	POLR2A	chr12:120636372-120639631	GM18505	blood:	n/a	n/a
32	POLR2A	chr12:120635694-120639558	GM12891	blood:	n/a	n/a
33	POLR2A	chr12:120632184-120639485	GM12891	blood:	n/a	n/a
34	USF2	chr12:120634750-120637072	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr12:120636039-120639896	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr12:120636203-120637529	GM12878	blood:	n/a	n/a
37	POLR2A	chr12:120636188-120637299	A549	lung:	n/a	n/a
38	POLR2A	chr12:120631828-120639777	PFSK-1	brain:	n/a	n/a
39	POLR2A	chr12:120632144-120640040	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr12:120636389-120636668	A549	lung:	n/a	n/a
41	POLR2A	chr12:120636139-120637511	ECC-1	luminal epithelium:	n/a	n/a
42	POLR2A	chr12:120636196-120639505	HepG2	liver:	n/a	n/a
43	POLR2A	chr12:120631997-120639698	GM12892	blood:	n/a	n/a
44	CTCF	chr12:120636201-120636574	T-47D	breast:	n/a	n/a
45	POLR2A	chr12:120636219-120637343	A549	lung:	n/a	n/a
46	POLR2A	chr12:120636132-120639593	GM12878	blood:	n/a	n/a
47	POLR2A	chr12:120632082-120639796	U87	brain:	n/a	n/a
48	POLR2A	chr12:120632292-120639373	K562	blood:	n/a	n/a
49	POLR2A	chr12:120636223-120639618	PBDE	blood:	n/a	n/a
50	POLR2A	chr12:120635609-120639934	K562	blood:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:120628864..120642103-chr12:120725347..120732286,54	K562	blood:
2	chr12:120628211..120641965-chr12:120660551..120674110,39	K562	blood:
3	chr12:120551826..120556882-chr12:120630846..120640383,26	K562	blood:
4	chr12:120634142..120641127-chr12:120698850..120705439,14	K562	blood:
5	chr12:120626707..120642605-chr12:120719450..120732919,96	MCF-7	breast:
6	chr12:120552903..120558662-chr12:120635855..120639972,12	MCF-7	breast:
7	chr12:120574814..120578175-chr12:120636472..120639249,3	MCF-7	breast:
8	chr12:120636290..120639093-chr17:59486664..59489640,2	MCF-7	breast:
9	chr12:120636466..120640337-chr12:120966729..120969535,3	MCF-7	breast:
10	chr12:120631139..120640506-chr12:120724902..120734482,54	K562	blood:
11	chr12:120636494..120638550-chr12:120756430..120759190,2	MCF-7	breast:
12	chr12:120635810..120640156-chr12:120882395..120885946,4	K562	blood:

No data

Variant related genes	Relation type
RPLP0	TF binding region
PXN-AS1	TF binding region
GCN1L1	TF binding region
ENSG00000110871	Chromatin interaction
ENSG00000257218	Chromatin interaction
ENSG00000111737	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000200795	Chromatin interaction
ENSG00000089159	Chromatin interaction
ENSG00000123009	Chromatin interaction
ENSG00000187013	Chromatin interaction
ENSG00000089154	Chromatin interaction
ENSG00000170855	Chromatin interaction
ENSG00000202538	Chromatin interaction

Extended variants
information (count: 76 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10437836	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10744748	0.82[JPT][hapmap]
rs11065035	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11065036	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11065040	0.90[ASN][1000 genomes]
rs1151824	0.85[CHB][hapmap];0.91[JPT][hapmap]
rs1151825	0.85[CHB][hapmap];0.91[JPT][hapmap]
rs1151827	0.85[CHB][hapmap];0.91[JPT][hapmap]
rs1151832	0.91[JPT][hapmap]
rs1151837	0.90[JPT][hapmap]
rs11833158	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11836049	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1183781	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs12305184	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12306075	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12310433	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12312562	0.83[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.80[YRI][hapmap];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12320253	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12578300	0.96[EUR][1000 genomes]
rs1634814	0.85[CHB][hapmap];0.91[JPT][hapmap]
rs2238155	0.92[CEU][hapmap];0.90[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2240312	0.95[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap]
rs2240314	0.80[EUR][1000 genomes]
rs2240315	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs2240317	0.89[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs2240318	0.89[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2240319	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2240320	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2240321	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2240322	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2240323	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.96[TSI][hapmap];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2240325	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2269940	1.00[CEU][hapmap];1.00[TSI][hapmap];0.86[EUR][1000 genomes]
rs2269941	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2269943	0.86[EUR][1000 genomes]
rs2269944	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2269945	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2283362	1.00[CEU][hapmap];0.81[CHD][hapmap];0.84[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.93[EUR][1000 genomes]
rs2283364	0.95[JPT][hapmap]
rs2286043	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2286044	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs2286045	0.90[EUR][1000 genomes]
rs2286049	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap];0.86[YRI][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2286050	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2286051	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2422	0.86[JPT][hapmap]
rs3742039	0.85[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap]
rs3742040	0.84[EUR][1000 genomes]
rs3815210	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3888586	0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs4522230	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57546423	0.88[EUR][1000 genomes]
rs57780521	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs59601514	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs60271600	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7133235	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7134706	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7135914	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7294892	0.87[EUR][1000 genomes]
rs7296380	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7299429	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7301660	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7310175	0.89[ASN][1000 genomes]
rs7953741	0.80[EUR][1000 genomes]
rs7974732	0.90[ASN][1000 genomes]
rs7978061	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7978175	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9630281	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9651914	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3525916	chr12:120345352-120665045	Bivalent Enhancer Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
2	esv3525917	chr12:120345352-120665045	Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Active 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	99 gene(s)	inside rSNPs	diseases
3	nsv899555	chr12:120519124-120840522	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	499 gene(s)	inside rSNPs	diseases
4	nsv519657	chr12:120533696-120676090	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv560433	chr12:120533696-120676090	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS 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	94 gene(s)	inside rSNPs	diseases
6	nsv832530	chr12:120586069-120758175	Flanking Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Active TSS 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	484 gene(s)	inside rSNPs	diseases
7	nsv973128	chr12:120635459-120637245	Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2074540	GCN1L1	cis	lymphoblastoid	seeQTL
rs2074540	FBXO21	cis	parietal	SCAN
rs2074540	GCN1L1	cis	Lymphoblastoid	GTEx
rs2074540	GCN1L1	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120633000-120637200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:120633000-120637800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr12:120633200-120638400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr12:120633400-120636800	Strong transcription	Fetal Stomach	stomach
5	chr12:120633400-120637200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr12:120633400-120637600	Genic enhancers	Liver	Liver
7	chr12:120633600-120637000	Genic enhancers	Fetal Thymus	thymus
8	chr12:120633600-120638000	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
9	chr12:120633600-120638200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:120633800-120636600	Strong transcription	Colonic Mucosa	Colon
11	chr12:120633800-120636800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr12:120633800-120636800	Strong transcription	Brain Anterior Caudate	brain
13	chr12:120633800-120636800	Strong transcription	Brain Hippocampus Middle	brain
14	chr12:120633800-120636800	Strong transcription	Fetal Intestine Large	intestine
15	chr12:120633800-120637200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr12:120633800-120637400	Strong transcription	Fetal Kidney	kidney
17	chr12:120633800-120637600	Genic enhancers	Placenta	Placenta
18	chr12:120633800-120638600	Transcr. at gene 5' and 3'	K562	blood
19	chr12:120634000-120636600	Strong transcription	Right Ventricle	heart
20	chr12:120634000-120636800	Strong transcription	Brain Cingulate Gyrus	brain
21	chr12:120634000-120636800	Strong transcription	Brain Substantia Nigra	brain
22	chr12:120634000-120636800	Strong transcription	Colon Smooth Muscle	Colon
23	chr12:120634000-120636800	Genic enhancers	Skeletal Muscle Female	skeletal muscle
24	chr12:120634000-120636800	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr12:120634000-120637000	Strong transcription	Brain Inferior Temporal Lobe	brain
26	chr12:120634000-120637000	Strong transcription	Placenta Amnion	Placenta Amnion
27	chr12:120634000-120637000	Strong transcription	Rectal Smooth Muscle	rectum
28	chr12:120634000-120637200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
29	chr12:120634000-120637200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:120634000-120637400	Strong transcription	Primary monocytes fromperipheralblood	blood
31	chr12:120634000-120637600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr12:120634200-120636600	Genic enhancers	HSMM	muscle
33	chr12:120634200-120636800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr12:120634200-120636800	Strong transcription	Sigmoid Colon	Sigmoid Colon
35	chr12:120634200-120637400	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr12:120634200-120637400	Strong transcription	Ovary	ovary
37	chr12:120634400-120636600	Strong transcription	Primary neutrophils fromperipheralblood	blood
38	chr12:120634400-120637800	Transcr. at gene 5' and 3'	Hela-S3	cervix
39	chr12:120634600-120637000	Strong transcription	Aorta	Aorta
40	chr12:120634600-120637400	Strong transcription	Esophagus	oesophagus
41	chr12:120634600-120637600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:120634800-120636800	Strong transcription	Brain Angular Gyrus	brain
43	chr12:120634800-120636800	Genic enhancers	Duodenum Smooth Muscle	Duodenum
44	chr12:120634800-120637200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr12:120634800-120637600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:120634800-120637600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
47	chr12:120634800-120638600	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
48	chr12:120634800-120638600	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
49	chr12:120634800-120638800	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
50	chr12:120635000-120637000	Strong transcription	Pancreatic Islets	Pancreatic Islet

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