Variant report

Variant	rs798490
Chromosome Location	chr7:2801542-2801543
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr7:2799243-2801814	SK-N-SH	brain:	n/a	chr7:2799554-2799564 chr7:2799556-2799570

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:2801509-2801559	HCPEpiC	choroid plexus:	n/a
2	chr7:2801509-2801559	PANC-1	pancreas:	n/a
3	chr7:2801509-2801559	HIPEpiC	eye:	n/a
4	chr7:2801509-2801559	HepG2	liver:	n/a
5	chr7:2801509-2801559	HRPEpiC	eye:	n/a
6	chr7:2801509-2801559	H1-hESC	embryonic stem cell:	embryo
7	chr7:2801509-2801559	Caco-2	colon:	n/a
8	chr7:2801509-2801559	GM19239	blood:	n/a
9	chr7:2801509-2801559	HRE	kidney:	n/a
10	chr7:2801509-2801559	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:2801509-2801559	GM06990	blood:	n/a
12	chr7:2801509-2801559	GM12878	blood:	n/a
13	chr7:2801509-2801559	A549	lung:	n/a
14	chr7:2801509-2801559	MCF10A-Er-Src	breast:	n/a
15	chr7:2801509-2801559	HL-60	blood:	n/a
16	chr7:2801509-2801559	HRCEpiC	kidney:	n/a
17	chr7:2801509-2801559	K562	blood:	n/a
18	chr7:2801509-2801559	SAEC	small airway:	n/a
19	chr7:2801509-2801559	BJ	skin:	n/a
20	chr7:2801509-2801559	NHDF-neo	bronchial:	n/a
21	chr7:2801509-2801559	T-47D	breast:	n/a
22	chr7:2801509-2801559	SK-N-MC	brain:	n/a
23	chr7:2801509-2801559	HCT-116	colon:	n/a
24	chr7:2801509-2801559	ProgFib	skin:	n/a
25	chr7:2801509-2801559	AoSMC	blood vessel:	n/a
26	chr7:2801509-2801559	Hela-S3	cervix:	n/a
27	chr7:2801509-2801559	SK-N-SH	brain:	n/a
28	chr7:2801509-2801559	CMK	blood:	n/a
29	chr7:2801509-2801559	HEK293	kidney:	embryo
30	chr7:2801509-2801559	LNCaP	prostate:	n/a
31	chr7:2801509-2801559	NB4	blood:	n/a
32	chr7:2801509-2801559	SKMC	muscle:	n/a
33	chr7:2801509-2801559	AG10803	skin:	n/a
34	chr7:2801509-2801559	GM12891	blood:	n/a
35	chr7:2801509-2801559	HUVEC	blood vessel:	n/a
36	chr7:2801509-2801559	HAEpiC	amniotic membrane:	n/a
37	chr7:2801509-2801559	AG09319	gingival:	n/a
38	chr7:2801509-2801559	HCM	heart:	n/a
39	chr7:2801509-2801559	U87	brain:	n/a
40	chr7:2801509-2801559	AG04450	lung:	fetal
41	chr7:2801509-2801559	IMR90	lung:	fetal
42	chr7:2801509-2801559	BE2_C	brain:	n/a
43	chr7:2801509-2801559	ECC-1	luminal epithelium:	n/a
44	chr7:2801509-2801559	NHBE	bronchial:	n/a
45	chr7:2801509-2801559	Hepatocyte	liver:	n/a
46	chr7:2801509-2801559	NT2-D1	testis:	n/a
47	chr7:2801509-2801559	HNPCEpiC	eye:	n/a
48	chr7:2801509-2801559	ovcar-3	ovarian:	n/a
49	chr7:2801509-2801559	PrEC	prostate:	n/a
50	chr7:2801509-2801559	NH-A	brain:	n/a

No data

Variant related genes	Relation type
AMZ1	TF binding region
GNA12	TF binding region
AMZ1	CpG island
GNA12	CpG island

Extended variants
information (count: 119 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs1182155	0.81[TSI][hapmap]
rs1182172	0.84[EUR][1000 genomes]
rs1182174	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs1182176	0.86[EUR][1000 genomes]
rs1182177	0.91[CEU][hapmap];0.85[JPT][hapmap];0.86[EUR][1000 genomes]
rs1182178	0.86[EUR][1000 genomes]
rs1182179	0.91[CEU][hapmap];0.85[GIH][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.86[EUR][1000 genomes]
rs1182181	0.91[CEU][hapmap];0.85[GIH][hapmap];0.85[JPT][hapmap];0.95[MEX][hapmap];0.94[TSI][hapmap];0.85[EUR][1000 genomes]
rs1182182	0.85[EUR][1000 genomes]
rs1182183	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs1182184	0.83[JPT][hapmap];0.85[EUR][1000 genomes]
rs1182185	0.90[CEU][hapmap];0.85[EUR][1000 genomes]
rs1182186	0.86[EUR][1000 genomes]
rs1182187	0.88[EUR][1000 genomes]
rs1182188	0.91[CEU][hapmap];0.85[GIH][hapmap];0.85[JPT][hapmap];0.95[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs1182189	0.91[CEU][hapmap];0.85[JPT][hapmap];0.87[EUR][1000 genomes]
rs1182191	0.84[JPT][hapmap]
rs1182196	0.84[CHB][hapmap];0.93[JPT][hapmap]
rs1182198	0.86[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1182199	0.81[EUR][1000 genomes]
rs1182207	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1182208	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1182209	0.94[CHB][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs1183085	0.85[JPT][hapmap];0.86[EUR][1000 genomes]
rs13243214	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1636249	0.81[TSI][hapmap]
rs1636250	0.81[TSI][hapmap]
rs1636255	0.82[CEU][hapmap];0.94[TSI][hapmap]
rs1636264	0.86[CEU][hapmap];0.84[CHB][hapmap];0.85[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap];0.91[MEX][hapmap];0.84[TSI][hapmap];0.81[EUR][1000 genomes]
rs1713919	0.91[CEU][hapmap];0.84[CHB][hapmap];0.85[JPT][hapmap];0.87[EUR][1000 genomes]
rs1713920	0.83[JPT][hapmap]
rs2107964	0.91[CEU][hapmap];0.84[CHB][hapmap];0.93[JPT][hapmap];0.84[EUR][1000 genomes]
rs2158694	0.86[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];0.87[EUR][1000 genomes]
rs2248390	0.81[ASN][1000 genomes]
rs2251491	0.81[ASN][1000 genomes]
rs2260230	1.00[CEU][hapmap];0.89[CHB][hapmap];0.92[JPT][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2266922	0.89[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs2283779	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2283783	0.81[ASN][1000 genomes]
rs2283784	0.81[ASN][1000 genomes]
rs2527683	0.90[ASN][1000 genomes]
rs2527684	0.89[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2527687	0.89[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2527690	0.82[ASN][1000 genomes]
rs2527692	0.81[ASN][1000 genomes]
rs2533870	0.81[TSI][hapmap]
rs2533878	0.91[CEU][hapmap];0.85[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.84[EUR][1000 genomes]
rs2533879	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2533882	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2533884	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2644274	0.89[CHB][hapmap];0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs2644275	0.89[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs2644281	0.81[TSI][hapmap]
rs2644294	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2644295	0.89[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap]
rs2644296	0.89[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap]
rs2644297	0.89[CHB][hapmap];0.93[JPT][hapmap]
rs2644312	0.91[CEU][hapmap];0.84[CHB][hapmap];0.92[JPT][hapmap];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35957220	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6970963	0.88[ASN][1000 genomes]
rs6978692	0.81[ASN][1000 genomes]
rs709282	0.89[ASN][1000 genomes]
rs757791	0.89[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap]
rs7777484	0.95[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs7783400	0.81[TSI][hapmap]
rs7807978	0.95[CHB][hapmap];1.00[CHD][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs798480	0.99[ASN][1000 genomes]
rs798481	0.83[ASN][1000 genomes]
rs798482	0.99[ASN][1000 genomes]
rs798485	0.86[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.96[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs798486	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs798487	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs798488	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs798489	0.91[CEU][hapmap];0.93[EUR][1000 genomes]
rs798491	0.95[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs798492	0.90[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs798493	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs798494	0.95[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs798495	0.95[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs798496	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs798497	0.87[ASW][hapmap];0.95[CEU][hapmap];0.90[CHB][hapmap];0.96[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs798498	0.91[CEU][hapmap];0.84[CHB][hapmap];0.93[JPT][hapmap];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs798499	0.84[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs798500	0.95[CEU][hapmap];0.84[CHB][hapmap];0.89[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs798502	0.91[CEU][hapmap];0.88[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs798506	0.88[EUR][1000 genomes]
rs798508	0.99[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs798511	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs798512	0.84[CHB][hapmap];0.86[JPT][hapmap];0.89[ASN][1000 genomes]
rs798513	0.89[ASN][1000 genomes]
rs798514	0.99[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs798518	0.82[CEU][hapmap];0.84[CHB][hapmap];0.92[JPT][hapmap];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs798526	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs798528	0.87[CEU][hapmap];0.84[CHB][hapmap];0.93[JPT][hapmap];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs798531	0.89[ASN][1000 genomes]
rs798536	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs798540	0.80[ASN][1000 genomes]
rs798547	0.82[ASN][1000 genomes]
rs798548	0.91[CEU][hapmap];0.89[CHD][hapmap];0.88[GIH][hapmap];0.95[MEX][hapmap]
rs798550	0.82[ASN][1000 genomes]
rs798551	0.82[ASN][1000 genomes]
rs798552	0.82[ASN][1000 genomes]
rs798554	0.86[CEU][hapmap];0.89[CHD][hapmap];0.88[GIH][hapmap];0.95[MEX][hapmap];0.82[ASN][1000 genomes]
rs798555	0.85[ASN][1000 genomes]
rs798556	0.86[CEU][hapmap];0.82[ASN][1000 genomes]
rs798557	0.89[CHB][hapmap];0.85[ASN][1000 genomes]
rs798558	0.82[ASN][1000 genomes]
rs798559	0.82[ASN][1000 genomes]
rs798560	0.82[ASN][1000 genomes]
rs798562	0.84[ASN][1000 genomes]
rs798565	0.82[AMR][1000 genomes]
rs960273	0.91[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.82[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	nsv1029250	chr7:2722737-2881021	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv538652	chr7:2722737-2881021	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1024023	chr7:2726210-2829581	Strong transcription Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv538653	chr7:2726210-2829581	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv1015700	chr7:2753965-2945848	Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Weak transcription Bivalent Enhancer 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 target site	30 gene(s)	inside rSNPs	diseases
6	nsv1032282	chr7:2789555-2820774	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1022612	chr7:2789555-3019200	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs798490	GNA12	cis	Nerve Tibial	GTEx
rs798490	LOC392620	cis	multi-tissue	Pritchard
rs798490	GNA12	cis	multi-tissue	Pritchard
rs798490	GNA12	cis	lymphoblastoid	seeQTL
rs798490	GNA12	cis	Artery Tibial	GTEx
rs798490		cis	Lymphoblastoid	GTEx
rs798490	C7orf27	cis	parietal	SCAN

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:2789200-2831600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr7:2790000-2830400	Weak transcription	Aorta	Aorta
3	chr7:2791200-2803400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr7:2796400-2801600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr7:2796400-2803200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr7:2796400-2804000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr7:2796800-2802000	Enhancers	Adipose Nuclei	Adipose
8	chr7:2796800-2803600	Weak transcription	Primary B cells from cord blood	blood
9	chr7:2796800-2804400	Enhancers	Fetal Muscle Leg	muscle
10	chr7:2797000-2801800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:2797000-2803200	Enhancers	Right Ventricle	heart
12	chr7:2797000-2803800	Enhancers	Brain Cingulate Gyrus	brain
13	chr7:2797000-2805400	Enhancers	Placenta	Placenta
14	chr7:2797600-2831200	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr7:2798000-2803600	Enhancers	Placenta Amnion	Placenta Amnion
16	chr7:2798000-2827400	Weak transcription	Thymus	Thymus
17	chr7:2798200-2803200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:2798400-2802000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:2798400-2802200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr7:2798400-2802200	Enhancers	Osteobl	bone
21	chr7:2798400-2803000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr7:2798600-2801600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:2798600-2802000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:2799000-2801600	Enhancers	Stomach Mucosa	stomach
25	chr7:2799000-2801800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr7:2799000-2803800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr7:2799200-2801800	Enhancers	Lung	lung
28	chr7:2799200-2802200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:2799200-2802400	Strong transcription	Primary B cells from peripheral blood	blood
30	chr7:2799200-2802400	Enhancers	Right Atrium	heart
31	chr7:2799200-2802600	Enhancers	Left Ventricle	heart
32	chr7:2799200-2804400	Enhancers	Ovary	ovary
33	chr7:2799200-2804600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr7:2799200-2817000	Weak transcription	Dnd41	blood
35	chr7:2799200-2827200	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr7:2799400-2801600	Genic enhancers	Spleen	Spleen
37	chr7:2799600-2802400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr7:2799600-2803800	Genic enhancers	Fetal Stomach	stomach
39	chr7:2799600-2807600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:2799600-2825600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr7:2800000-2801600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:2800200-2802200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:2800200-2802400	Enhancers	Brain Anterior Caudate	brain
44	chr7:2800200-2803600	Enhancers	Fetal Heart	heart
45	chr7:2800200-2806400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:2800200-2815800	Weak transcription	Liver	Liver
47	chr7:2800400-2802000	Genic enhancers	NHLF	lung
48	chr7:2800400-2802200	Weak transcription	HMEC	breast
49	chr7:2800400-2804400	Enhancers	NHDF-Ad	bronchial
50	chr7:2800400-2810200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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