Variant report

Variant	rs799488
Chromosome Location	chr14:35451410-35451411
allele	C/T
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	CHD2	chr14:35451317-35452461	H1-hESC	embryonic stem cell:	n/a	n/a
2	PBX3	chr14:35451367-35452510	SK-N-SH	brain:	n/a	chr14:35451593-35451613
3	MAX	chr14:35451081-35452563	K562	blood:	n/a	chr14:35452357-35452366 chr14:35451986-35451994
4	POLR2A	chr14:35451025-35452539	GM12892	blood:	n/a	n/a
5	POLR2A	chr14:35451112-35452534	HepG2	liver:	n/a	n/a
6	TAF1	chr14:35451230-35452331	SK-N-SH	brain:	n/a	n/a
7	NFIC	chr14:35451401-35452493	ECC-1	luminal epithelium:	n/a	n/a
8	TBP	chr14:35451336-35452731	GM12878	blood:	n/a	n/a
9	SIN3AK20	chr14:35451369-35452713	HepG2	liver:	n/a	n/a
10	POLR2A	chr14:35451015-35452569	GM12892	blood:	n/a	n/a
11	SP2	chr14:35451387-35452950	HepG2	liver:	n/a	n/a
12	CHD2	chr14:35451361-35452683	HepG2	liver:	n/a	n/a
13	ELF1	chr14:35451390-35452569	HepG2	liver:	n/a	chr14:35452139-35452148 chr14:35452134-35452143
14	ELF1	chr14:35451032-35452552	GM12878	blood:	n/a	chr14:35452139-35452148 chr14:35452134-35452143
15	EP300	chr14:35451364-35451910	T-47D	breast:	n/a	n/a
16	MYC	chr14:35451030-35452613	K562	blood:	n/a	chr14:35452357-35452366 chr14:35451986-35451994
17	CTCF	chr14:35451360-35451510	NHLF	lung:	n/a	n/a
18	FOXA1	chr14:35451343-35452594	HepG2	liver:	n/a	n/a
19	POLR2A	chr14:35449987-35452510	HepG2	liver:	n/a	n/a
20	MXI1	chr14:35450443-35452921	GM12878	blood:	n/a	n/a
21	RAD21	chr14:35451001-35451889	H1-hESC	embryonic stem cell:	n/a	n/a
22	CUX1	chr14:35451395-35452409	GM12878	blood:	n/a	n/a
23	HA-E2F1	chr14:35451123-35452656	MCF-7	breast:	n/a	chr14:35452436-35452443 chr14:35452436-35452443 chr14:35452431-35452446 chr14:35452435-35452447 chr14:35452435-35452444 chr14:35451773-35451782 chr14:35452436-35452443
24	SIN3AK20	chr14:35451235-35451653	A549	lung:	n/a	n/a
25	POLR2A	chr14:35451298-35452651	HL-60	blood:	n/a	n/a
26	RAD21	chr14:35450487-35452602	IMR90	lung:	n/a	chr14:35452231-35452245
27	ZNF143	chr14:35451001-35452390	K562	blood:	n/a	n/a
28	MAX	chr14:35451135-35452411	Hela-S3	cervix:	n/a	chr14:35452357-35452366 chr14:35451986-35451994
29	RAD21	chr14:35451287-35452427	HepG2	liver:	n/a	chr14:35452231-35452245
30	POLR2A	chr14:35451194-35452577	GM15510	blood:	n/a	n/a
31	MAX	chr14:35450382-35452619	NB4	blood:	n/a	chr14:35452357-35452366 chr14:35451986-35451994
32	POLR2A	chr14:35450835-35453495	H1-hESC	embryonic stem cell:	n/a	n/a
33	MAX	chr14:35451270-35452571	H1-hESC	embryonic stem cell:	n/a	chr14:35452357-35452366 chr14:35451986-35451994
34	POLR2A	chr14:35451287-35452785	HepG2	liver:	n/a	n/a
35	ATF3	chr14:35451382-35452359	A549	lung:	n/a	n/a
36	TBP	chr14:35451179-35452434	K562	blood:	n/a	n/a
37	UBTF	chr14:35451317-35452030	K562	blood:	n/a	n/a
38	RELA	chr14:35451273-35452498	GM10847	blood:	n/a	chr14:35452375-35452384 chr14:35452375-35452384
39	POLR2A	chr14:35450888-35452860	GM12878	blood:	n/a	n/a
40	PML	chr14:35451316-35452405	GM12878	blood:	n/a	n/a
41	MYC	chr14:35451107-35452688	K562	blood:	n/a	chr14:35452357-35452366 chr14:35451986-35451994
42	POLR2A	chr14:35451322-35452593	GM18951	blood:	n/a	n/a
43	POLR2A	chr14:35451212-35452474	U87	brain:	n/a	n/a
44	CTCF	chr14:35451400-35451550	A549	lung:	n/a	n/a
45	POLR2A	chr14:35451151-35452600	GM12892	blood:	n/a	n/a
46	KAP1	chr14:35449869-35452510	HEK293	kidney:	n/a	n/a
47	ATF2	chr14:35451408-35452422	H1-hESC	embryonic stem cell:	n/a	chr14:35452182-35452196
48	SIN3AK20	chr14:35451001-35452572	SK-N-SH	brain:	n/a	n/a
49	REST	chr14:35451178-35452525	A549	lung:	n/a	chr14:35451922-35451935 chr14:35451794-35451807 chr14:35452458-35452471
50	TAL1	chr14:35450628-35452136	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:35449513..35454029-chr14:35868261..35874094,7	MCF-7	breast:
2	chr14:35449656..35453109-chr14:35514529..35517063,4	MCF-7	breast:
3	chr14:35450596..35455465-chr14:35514082..35520003,7	MCF-7	breast:
4	chr1:201979282..201979938-chr14:35451253..35451757,2	Hela-S3	cervix:
5	chr14:35023701..35025768-chr14:35449276..35451419,2	K562	blood:
6	chr14:35341954..35346847-chr14:35449484..35456301,15	MCF-7	breast:
7	chr14:35450099..35453742-chr14:35513316..35517237,10	K562	blood:
8	chr14:35450376..35452323-chr14:35627573..35629639,2	K562	blood:
9	chr14:35451287..35451881-chr19:3557480..3558017,2	Hela-S3	cervix:
10	chr14:35341948..35345853-chr14:35449382..35453241,7	K562	blood:
11	chr14:35450245..35452169-chr14:35590215..35593362,3	MCF-7	breast:
12	chr14:35450146..35454994-chr14:35588530..35593322,8	MCF-7	breast:
13	chr14:35451366..35453471-chr14:35871625..35875238,3	MCF-7	breast:
14	chr10:52384532..52385151-chr14:35451145..35451802,2	Hela-S3	cervix:
15	chr14:35450042..35454830-chr14:35589505..35593708,8	K562	blood:
16	chr14:35341141..35345954-chr14:35450498..35453739,11	K562	blood:
17	chr14:35450019..35452754-chr14:35591061..35594828,4	K562	blood:
18	chr14:35341867..35346512-chr14:35447191..35456965,26	MCF-7	breast:
19	chr14:35451354..35452438-chr14:64971301..64972306,3	Hela-S3	cervix:
20	chr14:35449839..35454578-chr14:35513316..35515954,7	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAZ1A-1	chr14:35449441-35452103	NONHSAT036355

Variant related genes	Relation type
SRP54	TF binding region
ENSG00000258738	Chromatin interaction
ENSG00000163435	Chromatin interaction
ENSG00000198604	Chromatin interaction
ENSG00000100906	Chromatin interaction
ENSG00000206588	Chromatin interaction
ENSG00000092020	Chromatin interaction
ENSG00000267231	Chromatin interaction
ENSG00000100890	Chromatin interaction
ENSG00000151327	Chromatin interaction
ENSG00000258790	Chromatin interaction
ENSG00000234678	Chromatin interaction
ENSG00000226200	Chromatin interaction
ENSG00000126804	Chromatin interaction
ENSG00000161091	Chromatin interaction
ENSG00000198964	Chromatin interaction
ENSG00000089775	Chromatin interaction
ENSG00000259090	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10136692	1.00[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap];0.89[YRI][hapmap];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10151531	0.85[ASN][1000 genomes]
rs12892117	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1712356	0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1738798	0.88[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];0.93[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1741177	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs2747010	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28456062	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2982675	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs712314	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs712318	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7156361	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs799459	0.83[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];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs799464	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs799469	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs799473	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs799480	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs799484	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs799486	0.88[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];0.93[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs799495	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs799498	0.82[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];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs809584	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053722	chr14:35257458-35465784	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers 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	55 gene(s)	inside rSNPs	diseases
2	nsv1045939	chr14:35311074-35494703	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
3	nsv456203	chr14:35311272-35512335	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
4	nsv564200	chr14:35311272-35512335	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
5	nsv901602	chr14:35367889-35571651	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
6	nsv949617	chr14:35379923-35825436	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
7	nsv901604	chr14:35381137-35485748	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
8	nsv1043470	chr14:35398522-35754029	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
9	nsv542031	chr14:35398522-35754029	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS 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	65 gene(s)	inside rSNPs	diseases
10	nsv1035925	chr14:35404661-35483420	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
11	nsv901605	chr14:35409214-35512335	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
12	nsv901606	chr14:35449467-35512335	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
13	nsv901607	chr14:35449467-35540764	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers 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	48 gene(s)	inside rSNPs	diseases
14	nsv901608	chr14:35449467-35571651	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS 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	49 gene(s)	inside rSNPs	diseases
15	nsv901609	chr14:35449467-35587767	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs799488	C14orf24	cis	multi-tissue	Pritchard
rs799488	hmm3151	cis	multi-tissue	Pritchard
rs799488	C14orf126	cis	parietal	SCAN
rs799488	FAM177A1	cis	Lymphoblastoid	GTEx
rs799488	FAM177A1	cis	Whole Blood	GTEx
rs799488	FAM177A1	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35449600-35452800	Active TSS	Rectal Mucosa Donor 29	rectum
2	chr14:35449600-35453000	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr14:35449800-35452800	Active TSS	Hela-S3	cervix
4	chr14:35449800-35453000	Active TSS	NHEK	skin
5	chr14:35449800-35453000	Active TSS	Osteobl	bone
6	chr14:35449800-35453200	Active TSS	NHDF-Ad	bronchial
7	chr14:35449800-35453400	Active TSS	GM12878-XiMat	blood
8	chr14:35449800-35453600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr14:35449800-35453600	Active TSS	NHLF	lung
10	chr14:35449800-35455400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr14:35450000-35451600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
12	chr14:35450000-35451600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:35450000-35451600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:35450000-35452000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr14:35450000-35452800	Active TSS	HMEC	breast
16	chr14:35450000-35453000	Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr14:35450000-35453000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr14:35450000-35453000	Active TSS	Brain Angular Gyrus	brain
19	chr14:35450000-35453000	Active TSS	Fetal Intestine Large	intestine
20	chr14:35450000-35453000	Active TSS	A549	lung
21	chr14:35450000-35453200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr14:35450000-35453200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr14:35450000-35453200	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr14:35450000-35453200	Active TSS	NH-A	brain
25	chr14:35450000-35453400	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr14:35450000-35453600	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr14:35450000-35453600	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr14:35450200-35452800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr14:35450200-35453000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:35450200-35453000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr14:35450200-35453000	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr14:35450200-35453000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr14:35450200-35453000	Active TSS	Fetal Intestine Small	intestine
34	chr14:35450200-35453000	Active TSS	Stomach Mucosa	stomach
35	chr14:35450200-35453000	Bivalent/Poised TSS	HepG2	liver
36	chr14:35450200-35453200	Active TSS	H1 Cell Line	embryonic stem cell
37	chr14:35450200-35453200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr14:35450200-35453200	Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr14:35450200-35453200	Active TSS	Aorta	Aorta
40	chr14:35450200-35453200	Active TSS	HSMM	muscle
41	chr14:35450200-35453400	Active TSS	Right Atrium	heart
42	chr14:35450200-35453600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr14:35450200-35453600	Active TSS	Colonic Mucosa	Colon
44	chr14:35450200-35453800	Active TSS	K562	blood
45	chr14:35450400-35451600	Flanking Active TSS	Primary hematopoietic stem cells	blood
46	chr14:35450400-35451800	Flanking Active TSS	Adipose Nuclei	Adipose
47	chr14:35450400-35452200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr14:35450400-35452400	Active TSS	Thymus	Thymus
49	chr14:35450400-35452800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr14:35450400-35452800	Active TSS	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

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