Variant report

Variant	rs7151685
Chromosome Location	chr14:78225569-78225570
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr14:78224675-78225643	K562	blood:	n/a	n/a
2	POLR2A	chr14:78225563-78225788	HepG2	liver:	n/a	n/a
3	POLR2A	chr14:78224932-78225650	MCF10A-Er-Src	breast:	n/a	n/a
4	POLR2A	chr14:78225255-78225710	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:78225524-78225574	HMEC	breast:	n/a
2	chr14:78225551-78225601	HCPEpiC	choroid plexus:	n/a
3	chr14:78225524-78225574	AoSMC	blood vessel:	n/a
4	chr14:78225551-78225601	PrEC	prostate:	n/a
5	chr14:78225524-78225574	AG10803	skin:	n/a
6	chr14:78225551-78225601	HEK293	kidney:	embryo
7	chr14:78225524-78225574	HEK293	kidney:	embryo
8	chr14:78225551-78225601	NT2-D1	testis:	n/a
9	chr14:78225551-78225601	HRPEpiC	eye:	n/a
10	chr14:78225524-78225574	HCT-116	colon:	n/a
11	chr14:78225551-78225601	MCF-7	breast:	n/a
12	chr14:78225524-78225574	CMK	blood:	n/a
13	chr14:78225551-78225601	GM12892	blood:	n/a
14	chr14:78225551-78225601	BE2_C	brain:	n/a
15	chr14:78225524-78225574	GM19239	blood:	n/a
16	chr14:78225524-78225574	PrEC	prostate:	n/a
17	chr14:78225551-78225601	HUVEC	blood vessel:	n/a
18	chr14:78225524-78225574	NT2-D1	testis:	n/a
19	chr14:78225524-78225574	AG04450	lung:	fetal
20	chr14:78225524-78225574	SK-N-SH	brain:	n/a
21	chr14:78225524-78225574	SK-N-SH_RA	brain:	n/a
22	chr14:78225524-78225574	ProgFib	skin:	n/a
23	chr14:78225551-78225601	ovcar-3	ovarian:	n/a
24	chr14:78225551-78225601	HEEpiC	esophagus:	n/a
25	chr14:78225551-78225601	A549	lung:	n/a
26	chr14:78225551-78225601	HCF	heart:	n/a
27	chr14:78225551-78225601	H1-hESC	embryonic stem cell:	embryo
28	chr14:78225524-78225574	HRE	kidney:	n/a
29	chr14:78225524-78225574	HUVEC	blood vessel:	n/a
30	chr14:78225551-78225601	SK-N-MC	brain:	n/a
31	chr14:78225524-78225574	GM06990	blood:	n/a
32	chr14:78225551-78225601	GM19239	blood:	n/a
33	chr14:78225551-78225601	SAEC	small airway:	n/a
34	chr14:78225524-78225574	U87	brain:	n/a
35	chr14:78225524-78225574	ECC-1	luminal epithelium:	n/a
36	chr14:78225524-78225574	HEEpiC	esophagus:	n/a
37	chr14:78225551-78225601	AG09319	gingival:	n/a
38	chr14:78225551-78225601	MCF10A-Er-Src	breast:	n/a
39	chr14:78225551-78225601	GM12891	blood:	n/a
40	chr14:78225551-78225601	IMR90	lung:	fetal
41	chr14:78225524-78225574	HepG2	liver:	n/a
42	chr14:78225551-78225601	GM12878	blood:	n/a
43	chr14:78225551-78225601	HCT-116	colon:	n/a
44	chr14:78225551-78225601	HAEpiC	amniotic membrane:	n/a
45	chr14:78225524-78225574	BJ	skin:	n/a
46	chr14:78225524-78225574	HPAEpiC	pulmonary alveolar:	n/a
47	chr14:78225551-78225601	AG10803	skin:	n/a
48	chr14:78225551-78225601	RPTEC	kidney:	n/a
49	chr14:78225551-78225601	HPAEpiC	pulmonary alveolar:	n/a
50	chr14:78225524-78225574	SKMC	muscle:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:78223843..78225909-chr14:78468735..78470823,2	K562	blood:
2	chr14:78223413..78230716-chr14:78265065..78269735,15	MCF-7	breast:
3	chr14:78217096..78219959-chr14:78223868..78226613,3	K562	blood:
4	chr14:78003135..78004695-chr14:78224805..78226945,2	K562	blood:
5	chr14:78225549..78228360-chr14:78265163..78268062,4	K562	blood:

No data

Variant related genes	Relation type
C14orf178	TF binding region
C14orf178	CpG island
ENSG00000063761	Chromatin interaction

Extended variants
information (count: 105 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs1006038	0.90[CHB][hapmap]
rs1006039	0.90[CHB][hapmap]
rs1006040	0.90[CHB][hapmap]
rs1008988	0.95[CHB][hapmap]
rs10134425	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10138747	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10139492	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10142722	0.90[CHB][hapmap]
rs10143249	0.84[ASN][1000 genomes]
rs10143294	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10144448	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10146255	0.98[ASN][1000 genomes]
rs1048147	0.90[CHB][hapmap]
rs10483885	1.00[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs114763	1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs11621719	0.83[ASN][1000 genomes]
rs11622761	0.83[ASN][1000 genomes]
rs11624118	0.83[ASN][1000 genomes]
rs11628888	0.85[CHB][hapmap]
rs11846215	0.91[ASN][1000 genomes]
rs12879880	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12885306	1.00[CHB][hapmap];0.95[CHD][hapmap];0.84[JPT][hapmap]
rs12887313	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12890728	0.85[CHB][hapmap]
rs12890828	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1477262	0.90[CHB][hapmap]
rs1477263	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1477264	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17106157	0.90[CHB][hapmap]
rs176941	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs176943	0.90[CHB][hapmap]
rs176946	0.90[CHB][hapmap]
rs176947	0.87[ASN][1000 genomes]
rs176948	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs176951	0.90[CHB][hapmap]
rs176954	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs176955	0.90[CHB][hapmap]
rs176956	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs176959	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs176961	0.93[ASN][1000 genomes]
rs176963	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs176964	0.90[CHB][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs176965	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[LWK][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs176968	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs176969	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs176970	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs176972	0.92[ASN][1000 genomes]
rs176975	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs176976	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs176977	0.90[ASN][1000 genomes]
rs176980	0.90[CHB][hapmap]
rs2080703	0.87[ASN][1000 genomes]
rs2267756	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2267759	0.90[CHB][hapmap]
rs2267760	0.90[CHB][hapmap]
rs2267761	0.90[CHB][hapmap]
rs2267762	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2267763	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2267764	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2267766	0.87[AMR][1000 genomes]
rs2277917	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2284233	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2284234	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.92[YRI][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2284235	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.92[YRI][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2299930	0.90[CHB][hapmap]
rs3759728	0.90[CHB][hapmap]
rs3783980	0.90[CHB][hapmap]
rs3783981	0.87[ASN][1000 genomes]
rs3783982	0.87[ASN][1000 genomes]
rs4632066	0.90[CHB][hapmap]
rs4641655	0.98[ASN][1000 genomes]
rs4899670	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4899673	1.00[CHB][hapmap];0.97[CHD][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs4899674	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4903638	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992867	0.80[ASN][1000 genomes]
rs61992868	0.80[ASN][1000 genomes]
rs6574392	0.97[ASN][1000 genomes]
rs6574394	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6574399	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6574404	0.86[CHB][hapmap]
rs7142390	0.90[CHB][hapmap]
rs7143926	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7145717	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7148078	0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs7148126	0.87[ASN][1000 genomes]
rs7150531	0.96[ASN][1000 genomes]
rs7154571	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7159310	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7160355	0.96[ASN][1000 genomes]
rs717682	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs759713	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs8003691	0.90[CHB][hapmap]
rs8010541	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8011337	0.90[CHB][hapmap]
rs8015645	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs8016447	0.90[CHB][hapmap]
rs8022516	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9323649	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9323650	0.90[CHB][hapmap]
rs9323651	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];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758362	chr14:78074180-78262572	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	esv2759998	chr14:78074180-78262572	Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1043788	chr14:78178490-78381190	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	esv2754594	chr14:78222798-78275549	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs7151685	RPS6KL1	cis	cerebellum	SCAN
rs7151685	NEK9	cis	parietal	SCAN
rs7151685	ALDH6A1	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78201600-78226600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:78212800-78225600	Weak transcription	Stomach Mucosa	stomach
3	chr14:78214200-78226600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:78217000-78226600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr14:78218000-78226400	Weak transcription	Aorta	Aorta
6	chr14:78218200-78226400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr14:78218400-78226000	Weak transcription	Colonic Mucosa	Colon
8	chr14:78218400-78226400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr14:78219600-78225800	Weak transcription	HUVEC	blood vessel
10	chr14:78219800-78226400	Weak transcription	HSMM	muscle
11	chr14:78220000-78226000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr14:78221400-78226000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr14:78221400-78226400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr14:78221600-78225800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr14:78221600-78226000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:78221600-78226400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr14:78221600-78226600	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr14:78221800-78226200	Genic enhancers	Primary T cells fromperipheralblood	blood
19	chr14:78222000-78225800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
20	chr14:78222000-78226000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr14:78222600-78226200	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr14:78222800-78225600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr14:78222800-78226000	Weak transcription	Fetal Intestine Large	intestine
24	chr14:78223000-78226000	Weak transcription	Fetal Lung	lung
25	chr14:78223000-78226600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr14:78223200-78225600	Weak transcription	Fetal Intestine Small	intestine
27	chr14:78223200-78226600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:78223400-78225600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr14:78223400-78225600	Weak transcription	Fetal Muscle Trunk	muscle
30	chr14:78223400-78226200	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr14:78223400-78226200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr14:78223600-78226000	Genic enhancers	Primary B cells from peripheral blood	blood
33	chr14:78223600-78226200	Enhancers	Primary T cells from cord blood	blood
34	chr14:78223600-78226400	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr14:78223600-78226400	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr14:78223600-78226400	Enhancers	Adipose Nuclei	Adipose
37	chr14:78223800-78225800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr14:78223800-78225800	Genic enhancers	Dnd41	blood
39	chr14:78223800-78226000	Enhancers	Brain Germinal Matrix	brain
40	chr14:78223800-78226200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr14:78223800-78226400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr14:78224000-78226200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr14:78224200-78226400	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr14:78224600-78226400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr14:78224600-78226400	Enhancers	Psoas Muscle	Psoas
46	chr14:78224800-78225600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr14:78224800-78225600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr14:78224800-78225600	Genic enhancers	Brain Inferior Temporal Lobe	brain
49	chr14:78224800-78225600	Genic enhancers	Rectal Mucosa Donor 29	rectum
50	chr14:78224800-78225800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links