Variant report

Variant	rs2849030
Chromosome Location	chr11:62366986-62366987
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:197)
CpG islands
(count:0)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:197 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TBP	chr11:62366777-62366994	K562	blood:	n/a	n/a
2	POLR2A	chr11:62366540-62367009	K562	blood:	n/a	n/a
3	SIN3AK20	chr11:62366555-62367006	K562	blood:	n/a	n/a
4	POLR2A	chr11:62366356-62367015	HL-60	blood:	n/a	n/a
5	IRF4	chr11:62366507-62367030	GM12878	blood:	n/a	n/a
6	TBP	chr11:62366832-62367019	Hela-S3	cervix:	n/a	n/a
7	ARID3A	chr11:62366719-62367010	HepG2	liver:	n/a	n/a
8	RCOR1	chr11:62366495-62367099	K562	blood:	n/a	n/a
9	NFYA	chr11:62366604-62367062	K562	blood:	n/a	chr11:62366860-62366878 chr11:62366742-62366752 chr11:62366865-62366879
10	NFATC1	chr11:62366454-62367136	GM12878	blood:	n/a	n/a
11	MAX	chr11:62366473-62367160	SK-N-SH	brain:	n/a	n/a
12	NFIC	chr11:62366253-62367139	SK-N-SH	brain:	n/a	n/a
13	POLR2A	chr11:62366403-62367022	GM12891	blood:	n/a	n/a
14	SP1	chr11:62366469-62367093	HepG2	liver:	n/a	chr11:62366846-62366856 chr11:62366857-62366878 chr11:62366794-62366805 chr11:62366846-62366856
15	USF2	chr11:62366698-62367011	GM12878	blood:	n/a	n/a
16	NFYB	chr11:62366557-62366988	K562	blood:	n/a	chr11:62366742-62366752 chr11:62366865-62366879
17	MAX	chr11:62366525-62366991	K562	blood:	n/a	n/a
18	GABPA	chr11:62366473-62367167	SK-N-SH	brain:	n/a	chr11:62367150-62367159
19	MAX	chr11:62366686-62367006	HepG2	liver:	n/a	n/a
20	MAX	chr11:62366659-62367034	Hela-S3	cervix:	n/a	n/a
21	MXI1	chr11:62366539-62367050	K562	blood:	n/a	n/a
22	CHD2	chr11:62366521-62367043	GM12878	blood:	n/a	n/a
23	ZNF143	chr11:62366543-62367044	H1-hESC	embryonic stem cell:	n/a	n/a
24	YY1	chr11:62366522-62367027	GM12878	blood:	n/a	n/a
25	MYC	chr11:62366401-62367006	H1-hESC	embryonic stem cell:	n/a	n/a
26	MXI1	chr11:62366502-62367303	IMR90	lung:	n/a	n/a
27	POLR2A	chr11:62366513-62367043	K562	blood:	n/a	n/a
28	IRF1	chr11:62366531-62367098	K562	blood:	n/a	n/a
29	POLR2A	chr11:62366105-62367187	HUVEC	blood vessel:	n/a	n/a
30	NFATC1	chr11:62366437-62367039	GM12878	blood:	n/a	n/a
31	CEBPB	chr11:62366662-62366997	IMR90	lung:	n/a	n/a
32	TEAD4	chr11:62366599-62367110	HepG2	liver:	n/a	n/a
33	TBL1XR1	chr11:62366553-62367073	GM12878	blood:	n/a	n/a
34	SP1	chr11:62366226-62367302	HCT-116	colon:	n/a	chr11:62366846-62366856 chr11:62366857-62366878 chr11:62367145-62367157 chr11:62366794-62366805 chr11:62367146-62367155 chr11:62366846-62366856
35	BHLHE40	chr11:62366423-62367083	GM12878	blood:	n/a	n/a
36	MYBL2	chr11:62366457-62367230	HepG2	liver:	n/a	n/a
37	SIN3A	chr11:62366581-62367045	H1-hESC	embryonic stem cell:	n/a	chr11:62366881-62366894
38	MYC	chr11:62366527-62367052	K562	blood:	n/a	n/a
39	POLR2A	chr11:62366387-62367113	HUVEC	blood vessel:	n/a	n/a
40	MXI1	chr11:62366560-62367036	Hela-S3	cervix:	n/a	n/a
41	MAX	chr11:62366518-62367095	SK-N-SH	brain:	n/a	n/a
42	HDAC2	chr11:62366519-62367056	HepG2	liver:	n/a	n/a
43	HCFC1	chr11:62366747-62367036	K562	blood:	n/a	n/a
44	MAX	chr11:62366543-62367056	A549	lung:	n/a	n/a
45	GABPA	chr11:62366482-62367142	A549	lung:	n/a	n/a
46	MAX	chr11:62366543-62367083	ECC-1	luminal epithelium:	n/a	n/a
47	POLR2A	chr11:62366282-62367004	HCT-116	colon:	n/a	n/a
48	GATA1	chr11:62366744-62368510	PBDE	blood:	n/a	chr11:62368255-62368276 chr11:62368262-62368269 chr11:62367106-62367114 chr11:62368260-62368270 chr11:62367399-62367408 chr11:62368262-62368272 chr11:62368257-62368273 chr11:62368260-62368269
49	POLR2A	chr11:62366144-62367078	GM12892	blood:	n/a	n/a
50	SP4	chr11:62366519-62367092	H1-hESC	embryonic stem cell:	n/a	chr11:62366794-62366805

No data

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:62366402..62370002-chr11:62419166..62421218,5	MCF-7	breast:
2	chr11:62365951..62369565-chr11:62622521..62625872,5	K562	blood:
3	chr11:62366839..62369029-chr11:62472927..62475049,2	MCF-7	breast:
4	chr11:62365424..62367728-chr11:62413589..62415522,2	K562	blood:
5	chr11:62365249..62367009-chr11:62521402..62523143,2	K562	blood:
6	chr11:62366079..62370074-chr11:62386678..62390504,7	MCF-7	breast:
7	chr11:62340363..62343212-chr11:62365252..62369475,4	MCF-7	breast:
8	chr11:62362631..62371847-chr11:62427548..62442313,26	MCF-7	breast:
9	chr11:62366750..62367416-chr11:62379616..62380490,3	MCF-7	breast:
10	chr11:62365870..62369296-chr11:62605447..62609594,6	K562	blood:
11	chr11:62366145..62371000-chr11:62493302..62496531,6	K562	blood:
12	chr11:62366894..62368811-chr11:62572540..62574175,2	MCF-7	breast:
13	chr11:62365873..62371127-chr11:62605447..62611263,11	K562	blood:
14	chr11:62361223..62372590-chr11:62430599..62435389,30	K562	blood:
15	chr11:62366089..62368766-chr11:62475317..62477241,2	MCF-7	breast:
16	chr11:62365667..62370630-chr11:62493549..62497299,5	MCF-7	breast:
17	chr11:62355264..62375429-chr11:62428418..62443271,77	MCF-7	breast:
18	chr11:62365983..62370724-chr11:62412063..62418373,9	K562	blood:
19	chr11:62366955..62369844-chr11:62535933..62538904,2	K562	blood:
20	chr11:62365338..62373022-chr11:62621930..62625872,13	K562	blood:
21	chr11:62363464..62373052-chr11:62429645..62434985,23	K562	blood:
22	chr11:62344267..62349689-chr11:62366431..62369887,5	MCF-7	breast:
23	chr11:62365089..62370067-chr11:62436026..62441323,7	K562	blood:
24	chr11:62366910..62368974-chr11:62608295..62610836,2	MCF-7	breast:
25	chr11:62364986..62367408-chr11:62393044..62395358,2	MCF-7	breast:
26	chr11:62366689..62370631-chr11:62475430..62478411,3	MCF-7	breast:
27	chr11:62365885..62368421-chr11:62552476..62555212,3	K562	blood:

No data

Variant related genes	Relation type
MTA2	TF binding region
ENSG00000214756	Chromatin interaction
ENSG00000089597	Chromatin interaction
ENSG00000149016	Chromatin interaction
ENSG00000162231	Chromatin interaction
ENSG00000149499	Chromatin interaction
ENSG00000204922	Chromatin interaction
ENSG00000162222	Chromatin interaction
ENSG00000206597	Chromatin interaction
ENSG00000255432	Chromatin interaction
ENSG00000185670	Chromatin interaction
ENSG00000149489	Chromatin interaction
ENSG00000269176	Chromatin interaction
ENSG00000185085	Chromatin interaction
ENSG00000168000	Chromatin interaction
ENSG00000254772	Chromatin interaction
ENSG00000255717	Chromatin interaction
ENSG00000255508	Chromatin interaction
ENSG00000234857	Chromatin interaction
ENSG00000185475	Chromatin interaction
ENSG00000168003	Chromatin interaction
ENSG00000162227	Chromatin interaction
ENSG00000149541	Chromatin interaction
ENSG00000162194	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000214753	Chromatin interaction

Extended variants
information (count: 63 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1061093	0.87[EUR][1000 genomes]
rs11231138	0.96[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs11231141	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.87[EUR][1000 genomes]
rs11231144	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.87[EUR][1000 genomes]
rs11231145	0.87[EUR][1000 genomes]
rs11231150	0.96[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11231151	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11231152	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11231154	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11231155	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231156	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.97[TSI][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11231161	1.00[CEU][hapmap];0.88[CHB][hapmap];0.91[CHD][hapmap];0.97[GIH][hapmap];0.93[TSI][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11231176	1.00[JPT][hapmap]
rs11553576	1.00[CEU][hapmap];0.94[GIH][hapmap];0.88[TSI][hapmap];0.89[EUR][1000 genomes]
rs12049914	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12223627	0.88[ASN][1000 genomes]
rs12225213	0.96[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12226821	0.88[ASN][1000 genomes]
rs12808829	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13941	0.86[YRI][hapmap]
rs17773169	0.96[CEU][hapmap];0.88[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.93[TSI][hapmap];0.86[EUR][1000 genomes]
rs1801144	0.88[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes]
rs2428548	0.92[CEU][hapmap];0.88[CHB][hapmap]
rs2428549	0.92[CEU][hapmap];0.86[CHB][hapmap]
rs2428551	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2509961	0.92[CEU][hapmap];0.88[CHB][hapmap];0.89[GIH][hapmap];0.93[MEX][hapmap]
rs2509982	0.92[CEU][hapmap];0.88[CHB][hapmap]
rs2512562	0.92[CEU][hapmap];0.88[CHB][hapmap]
rs2512563	0.96[CEU][hapmap];0.88[CHB][hapmap]
rs2516633	1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.86[MKK][hapmap];0.88[TSI][hapmap];1.00[ASN][1000 genomes]
rs2516634	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2849031	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];0.93[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34065644	0.88[ASN][1000 genomes]
rs34894392	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35156678	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.97[TSI][hapmap]
rs35587183	0.88[CHB][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap]
rs35880596	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3923805	0.81[ASN][1000 genomes]
rs489778	0.85[YRI][hapmap]
rs58720921	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61296092	0.87[EUR][1000 genomes]
rs644616	0.86[YRI][hapmap]
rs67308910	0.85[ASN][1000 genomes]
rs693698	0.86[YRI][hapmap]
rs7124057	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.89[EUR][1000 genomes]
rs71490390	0.86[EUR][1000 genomes]
rs71490392	0.82[EUR][1000 genomes]
rs71490394	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72927213	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7928833	0.90[EUR][1000 genomes]
rs7930896	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.86[EUR][1000 genomes]
rs7937146	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7942991	0.88[CHB][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap]
rs7943191	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915636	chr11:62016992-62713565	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1441 gene(s)	inside rSNPs	diseases
2	nsv532283	chr11:62201358-62863475	Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1433 gene(s)	inside rSNPs	diseases
3	nsv532284	chr11:62220043-62630253	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1401 gene(s)	inside rSNPs	diseases
4	esv3584599	chr11:62262742-62398050	Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
5	nsv832182	chr11:62295575-62462848	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
6	nsv825939	chr11:62326083-62410577	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
7	nsv497903	chr11:62330308-62608042	Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	489 gene(s)	inside rSNPs	diseases
8	nsv555174	chr11:62334096-62496519	Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	243 gene(s)	inside rSNPs	diseases
9	nsv897622	chr11:62366986-62392229	Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs2849030	SLC22A9	cis	parietal	SCAN
rs2849030	EML3	cis	Whole Blood	GTEx
rs2849030	SLC22A25	cis	parietal	SCAN
rs2849030	SCYL1	cis	parietal	SCAN
rs2849030	EEF1G///LOC729998	N/A	lymphoblastoid	RTeQTL
rs2849030	EML3	cis	Esophagus Mucosa	GTEx
rs2849030	ROM1	cis	Thyroid	GTEx
rs2849030	CFL1	cis	parietal	SCAN
rs2849030	MTA2	cis	Esophagus Mucosa	GTEx
rs2849030	C11orf48	cis	cerebellum	SCAN
rs2849030	EML3	cis	cerebellum	SCAN
rs2849030	TUT1	cis	parietal	SCAN
rs2849030	EEF1G	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:62359800-62368200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:62360200-62367200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:62360200-62367200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:62360400-62367400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:62364600-62367200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:62365000-62367000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr11:62365000-62368000	Transcr. at gene 5' and 3'	Hela-S3	cervix
8	chr11:62365200-62368200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:62365400-62367200	Weak transcription	Small Intestine	intestine
10	chr11:62365400-62367400	Genic enhancers	Skeletal Muscle Female	skeletal muscle
11	chr11:62365600-62367800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
12	chr11:62365800-62367200	Genic enhancers	Fetal Muscle Trunk	muscle
13	chr11:62365800-62367400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr11:62366000-62367200	Genic enhancers	Fetal Muscle Leg	muscle
15	chr11:62366000-62367400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:62366000-62367400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr11:62366000-62367400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr11:62366000-62367400	Genic enhancers	Fetal Stomach	stomach
19	chr11:62366000-62368000	Weak transcription	Gastric	stomach
20	chr11:62366000-62368200	Transcr. at gene 5' and 3'	K562	blood
21	chr11:62366200-62367000	Genic enhancers	HUES64 Cell Line	embryonic stem cell
22	chr11:62366200-62367000	Transcr. at gene 5' and 3'	Primary B cells from peripheral blood	blood
23	chr11:62366200-62367200	Enhancers	Fetal Lung	lung
24	chr11:62366200-62367400	Genic enhancers	H1 Cell Line	embryonic stem cell
25	chr11:62366200-62367400	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr11:62366200-62367400	Genic enhancers	Fetal Intestine Small	intestine
27	chr11:62366200-62367400	Genic enhancers	Rectal Mucosa Donor 31	rectum
28	chr11:62366200-62367600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:62366200-62367800	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
30	chr11:62366200-62367800	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
31	chr11:62366200-62367800	Transcr. at gene 5' and 3'	HUVEC	blood vessel
32	chr11:62366200-62367800	Transcr. at gene 5' and 3'	NH-A	brain
33	chr11:62366200-62367800	Transcr. at gene 5' and 3'	Osteobl	bone
34	chr11:62366200-62368000	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
35	chr11:62366200-62368200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
36	chr11:62366200-62368200	Transcr. at gene 5' and 3'	A549	lung
37	chr11:62366200-62368200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr11:62366200-62368400	Flanking Active TSS	Primary hematopoietic stem cells	blood
39	chr11:62366200-62368400	Transcr. at gene 5' and 3'	Dnd41	blood
40	chr11:62366400-62367000	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr11:62366400-62367000	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr11:62366400-62367000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr11:62366400-62367000	Flanking Active TSS	Brain Angular Gyrus	brain
44	chr11:62366400-62367000	Transcr. at gene 5' and 3'	NHEK	skin
45	chr11:62366400-62367200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr11:62366400-62367200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr11:62366400-62367200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr11:62366400-62367200	Enhancers	Fetal Heart	heart
49	chr11:62366400-62367200	Active TSS	Fetal Kidney	kidney
50	chr11:62366400-62367400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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