Variant report

Variant	rs11149970
Chromosome Location	chr16:77225718-77225719
allele	C/G
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	MAZ	chr16:77224265-77226878	IMR90	lung:	n/a	n/a
2	STAT5A	chr16:77224678-77225842	GM12878	blood:	n/a	chr16:77225036-77225059 chr16:77225657-77225669 chr16:77225705-77225712
3	POLR2A	chr16:77224094-77225735	GM12878	blood:	n/a	n/a
4	POLR2A	chr16:77223958-77226689	MCF10A-Er-Src	breast:	n/a	n/a
5	MXI1	chr16:77224183-77225745	HepG2	liver:	n/a	n/a
6	POLR2A	chr16:77223956-77225823	GM12892	blood:	n/a	n/a
7	E2F6	chr16:77225306-77225732	K562	blood:	n/a	chr16:77225711-77225720
8	POLR2A	chr16:77223928-77228004	GM12878	blood:	n/a	n/a
9	SPI1	chr16:77225501-77225838	GM12891	blood:	n/a	n/a
10	SPI1	chr16:77225530-77225793	K562	blood:	n/a	n/a
11	POLR2A	chr16:77224737-77225740	HL-60	blood:	n/a	n/a
12	GABPA	chr16:77224188-77225748	A549	lung:	n/a	n/a
13	POLR2A	chr16:77224070-77225803	GM12878	blood:	n/a	n/a
14	POLR2A	chr16:77223991-77225829	GM18951	blood:	n/a	n/a
15	POLR2A	chr16:77224315-77225788	HL-60	blood:	n/a	n/a
16	CBX3	chr16:77225274-77225881	K562	blood:	n/a	n/a
17	POLR2A	chr16:77224265-77225852	GM12891	blood:	n/a	n/a
18	POLR2A	chr16:77224016-77225837	GM19193	blood:	n/a	n/a
19	GABPA	chr16:77223878-77225938	MCF-7	breast:	n/a	n/a
20	EP300	chr16:77224475-77225939	K562	blood:	n/a	chr16:77225054-77225061 chr16:77225025-77225032 chr16:77225083-77225090
21	POLR2A	chr16:77224060-77225879	Hela-S3	cervix:	n/a	n/a
22	MAX	chr16:77225390-77225754	HepG2	liver:	n/a	chr16:77225677-77225687
23	POLR2A	chr16:77223972-77226049	GM12892	blood:	n/a	n/a
24	RELA	chr16:77224284-77225866	GM15510	blood:	n/a	n/a
25	SPI1	chr16:77225498-77225850	GM12878	blood:	n/a	n/a
26	MYC	chr16:77224411-77225935	K562	blood:	n/a	chr16:77225677-77225687
27	RELA	chr16:77224416-77225799	GM18505	blood:	n/a	n/a
28	TBP	chr16:77224014-77225869	K562	blood:	n/a	n/a
29	POLR2A	chr16:77224307-77225975	GM12878	blood:	n/a	n/a
30	POLR2A	chr16:77224298-77225912	K562	blood:	n/a	n/a
31	MAX	chr16:77224197-77225880	NB4	blood:	n/a	chr16:77225677-77225687
32	NR2F2	chr16:77225431-77225815	K562	blood:	n/a	n/a
33	POLR2A	chr16:77224691-77225918	GM12891	blood:	n/a	n/a
34	MAX	chr16:77224123-77225867	MCF-7	breast:	n/a	chr16:77225677-77225687
35	POLR2A	chr16:77224022-77225905	GM18526	blood:	n/a	n/a
36	MAZ	chr16:77224054-77225849	K562	blood:	n/a	n/a
37	SMARCC1	chr16:77224066-77225913	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr16:77224070-77225753	GM12878	blood:	n/a	n/a
39	ATF2	chr16:77225510-77225842	GM12878	blood:	n/a	n/a
40	POLR2A	chr16:77224203-77226045	K562	blood:	n/a	n/a
41	MAX	chr16:77225332-77225814	K562	blood:	n/a	chr16:77225677-77225687
42	POLR2A	chr16:77224033-77226038	GM15510	blood:	n/a	n/a
43	MYC	chr16:77224335-77226093	K562	blood:	n/a	chr16:77225677-77225687
44	MYC	chr16:77225650-77225894	MCF10A-Er-Src	breast:	n/a	chr16:77225677-77225687
45	MYC	chr16:77224101-77225870	NB4	blood:	n/a	chr16:77225677-77225687
46	NR2F2	chr16:77224501-77225880	K562	blood:	n/a	n/a
47	ATF1	chr16:77225513-77225821	K562	blood:	n/a	n/a
48	MTA3	chr16:77224743-77225950	GM12878	blood:	n/a	n/a
49	SMARCB1	chr16:77224042-77225749	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr16:77224172-77226012	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:77223598..77226407-chr16:77245076..77246907,2	MCF-7	breast:
2	chr16:77223287..77227235-chr16:77231893..77237199,5	MCF-7	breast:
3	chr12:46121915..46124342-chr16:77224976..77226839,2	K562	blood:
4	chr16:77223216..77226884-chr16:77251990..77255920,6	MCF-7	breast:
5	chr16:77224879..77225863-chr4:151936610..151937513,2	Hela-S3	cervix:
6	chr16:75680522..75683233-chr16:77224728..77226496,3	MCF-7	breast:
7	chr16:75680135..75682966-chr16:77223241..77226200,3	MCF-7	breast:
8	chr16:77223534..77226455-chr16:77227601..77231752,9	MCF-7	breast:
9	chr1:200638562..200641266-chr16:77224293..77226737,2	MCF-7	breast:
10	chr16:77223627..77226316-chr16:77230976..77234622,5	MCF-7	breast:
11	chr16:77225300..77227094-chr16:77244120..77246217,2	MCF-7	breast:
12	chr16:77223923..77226639-chr16:77244818..77248823,8	K562	blood:
13	chr16:77224814..77227187-chr16:77245098..77247161,3	K562	blood:

Variant related genes	Relation type
MON1B	TF binding region
ENSG00000189079	Chromatin interaction
ENSG00000065427	Chromatin interaction
ENSG00000118197	Chromatin interaction
ENSG00000166848	Chromatin interaction
ENSG00000103111	Chromatin interaction
ENSG00000198589	Chromatin interaction
ENSG00000205078	Chromatin interaction
ENSG00000260088	Chromatin interaction
ENSG00000226348	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10781982	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11149972	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11149975	0.83[ASN][1000 genomes]
rs11639911	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11649440	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12447059	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12448094	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12716823	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2113282	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2232504	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2232509	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2241415	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2241416	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2278045	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34143201	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35660173	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3743759	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3743761	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3743762	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3760004	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3760005	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3760006	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3760007	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4887893	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62049594	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62049596	0.95[ASN][1000 genomes]
rs6420403	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6564404	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6564405	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6564406	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6564407	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6564408	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6564414	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7185297	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7185889	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7194408	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7195255	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7202265	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7204238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7205119	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8047912	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8048285	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8052509	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8062063	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9923489	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9924160	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9924694	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9930201	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9930541	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9939130	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9939212	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[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	nsv869201	chr16:76714549-77233646	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv1057677	chr16:76861946-77230013	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1065343	chr16:76927295-77279747	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv542965	chr16:76927295-77279747	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv1055234	chr16:77003426-77467286	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
6	nsv1065048	chr16:77003426-77675163	Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
7	esv2830376	chr16:77014551-77658185	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
8	nsv1065149	chr16:77032082-77671890	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
9	nsv1062349	chr16:77039764-77458731	Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
10	nsv542967	chr16:77039764-77458731	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer 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	27 gene(s)	inside rSNPs	diseases
11	nsv1056676	chr16:77139682-77854848	Strong transcription Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
12	nsv906954	chr16:77197633-77227180	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
13	nsv827756	chr16:77198788-77225812	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
14	nsv906955	chr16:77202701-77227180	Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
15	esv11803	chr16:77224589-77227011	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11149970	MON1B	cis	Whole Blood	GTEx
rs11149970	SYCE1L	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:77223200-77226200	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr16:77223400-77226600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:77223600-77226200	Active TSS	H1 Cell Line	embryonic stem cell
4	chr16:77223800-77225800	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr16:77223800-77225800	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr16:77223800-77225800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr16:77223800-77225800	Active TSS	Placenta Amnion	Placenta Amnion
8	chr16:77223800-77226000	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr16:77223800-77226000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr16:77223800-77226000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr16:77223800-77226000	Active TSS	GM12878-XiMat	blood
12	chr16:77223800-77226000	Active TSS	K562	blood
13	chr16:77223800-77226200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
14	chr16:77223800-77226600	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr16:77224000-77225800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr16:77224000-77225800	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr16:77224000-77225800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr16:77224000-77225800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr16:77224000-77225800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr16:77224000-77225800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr16:77224000-77225800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
22	chr16:77224000-77225800	Active TSS	Aorta	Aorta
23	chr16:77224000-77225800	Active TSS	Brain Substantia Nigra	brain
24	chr16:77224000-77225800	Active TSS	Esophagus	oesophagus
25	chr16:77224000-77225800	Active TSS	Fetal Intestine Small	intestine
26	chr16:77224000-77225800	Active TSS	Gastric	stomach
27	chr16:77224000-77225800	Active TSS	Lung	lung
28	chr16:77224000-77225800	Active TSS	Sigmoid Colon	Sigmoid Colon
29	chr16:77224000-77225800	Active TSS	A549	lung
30	chr16:77224000-77225800	Bivalent/Poised TSS	HepG2	liver
31	chr16:77224000-77226000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr16:77224000-77226000	Active TSS	H9 Cell Line	embryonic stem cell
33	chr16:77224000-77226000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr16:77224000-77226000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr16:77224000-77226000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr16:77224000-77226000	Active TSS	Brain Angular Gyrus	brain
37	chr16:77224000-77226000	Active TSS	Colonic Mucosa	Colon
38	chr16:77224000-77226000	Active TSS	Duodenum Mucosa	Duodenum
39	chr16:77224000-77226000	Active TSS	Ovary	ovary
40	chr16:77224000-77226000	Active TSS	Small Intestine	intestine
41	chr16:77224000-77226200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr16:77224000-77226200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr16:77224000-77226200	Active TSS	Fetal Intestine Large	intestine
44	chr16:77224000-77226200	Active TSS	Psoas Muscle	Psoas
45	chr16:77224000-77226200	Active TSS	Right Atrium	heart
46	chr16:77224000-77226200	Active TSS	NHDF-Ad	bronchial
47	chr16:77224000-77226400	Active TSS	Fetal Kidney	kidney
48	chr16:77224200-77225800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr16:77224200-77226200	Active TSS	HSMMtube	muscle
50	chr16:77224400-77225800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links