Variant report

Variant	rs11603384
Chromosome Location	chr11:63949095-63949096
allele	A/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	ETS1	chr11:63948936-63949347	A549	lung:	n/a	n/a
2	USF1	chr11:63948863-63949479	A549	lung:	n/a	chr11:63949187-63949200 chr11:63949189-63949198 chr11:63949187-63949198 chr11:63949188-63949197 chr11:63949189-63949198
3	ATF3	chr11:63949013-63949362	H1-hESC	embryonic stem cell:	n/a	chr11:63949189-63949209 chr11:63949189-63949198
4	JUND	chr11:63948962-63949313	HepG2	liver:	n/a	chr11:63949047-63949057 chr11:63949047-63949057 chr11:63949047-63949057 chr11:63949170-63949181
5	THAP1	chr11:63949011-63949202	K562	blood:	n/a	n/a
6	POLR2A	chr11:63948929-63949446	K562	blood:	n/a	n/a
7	NANOG	chr11:63949055-63949261	H1-hESC	embryonic stem cell:	n/a	n/a
8	JUND	chr11:63948917-63949455	K562	blood:	n/a	chr11:63949047-63949057 chr11:63949047-63949057 chr11:63949047-63949057 chr11:63949170-63949181
9	NR3C1	chr11:63948914-63949357	A549	lung:	n/a	n/a
10	MXI1	chr11:63949041-63949433	GM12878	blood:	n/a	n/a
11	POLR2A	chr11:63948911-63949403	Gliobla	brain:	n/a	n/a
12	YY1	chr11:63948920-63949303	A549	lung:	n/a	n/a
13	GTF2B	chr11:63949002-63949339	K562	blood:	n/a	n/a
14	TCF12	chr11:63949027-63949216	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr11:63948516-63949829	K562	blood:	n/a	n/a
16	USF1	chr11:63948973-63949439	SK-N-SH_RA	brain:	n/a	chr11:63949187-63949200 chr11:63949189-63949198 chr11:63949187-63949198 chr11:63949188-63949197 chr11:63949189-63949198
17	FOSL1	chr11:63949013-63949380	K562	blood:	n/a	chr11:63949047-63949057 chr11:63949047-63949057 chr11:63949047-63949057
18	NR2F2	chr11:63948874-63949645	K562	blood:	n/a	n/a
19	MAX	chr11:63948887-63949436	HepG2	liver:	n/a	chr11:63949189-63949198 chr11:63949189-63949198 chr11:63949187-63949200
20	MXI1	chr11:63949027-63949422	K562	blood:	n/a	n/a
21	CEBPD	chr11:63948950-63949332	HepG2	liver:	n/a	n/a
22	FOSL2	chr11:63948796-63949500	SK-N-SH	brain:	n/a	chr11:63949047-63949057 chr11:63949047-63949057 chr11:63949047-63949057
23	POLR2A	chr11:63948827-63949479	ProgFib	skin:	n/a	n/a
24	TAF1	chr11:63948950-63949410	H1-hESC	embryonic stem cell:	n/a	n/a
25	RUNX3	chr11:63948948-63949349	GM12878	blood:	n/a	n/a
26	USF2	chr11:63948897-63949454	Hela-S3	cervix:	n/a	chr11:63949187-63949200 chr11:63949189-63949198 chr11:63949188-63949197 chr11:63949187-63949198 chr11:63949189-63949198
27	BHLHE40	chr11:63949008-63949406	GM12878	blood:	n/a	chr11:63949187-63949200 chr11:63949189-63949198 chr11:63949188-63949197 chr11:63949189-63949198
28	POLR2A	chr11:63948832-63949468	U87	brain:	n/a	n/a
29	MAX	chr11:63948915-63949377	ECC-1	luminal epithelium:	n/a	chr11:63949189-63949198 chr11:63949189-63949198 chr11:63949187-63949200
30	REST	chr11:63948975-63949329	SK-N-SH	brain:	n/a	n/a
31	BHLHE40	chr11:63948991-63949408	HepG2	liver:	n/a	chr11:63949187-63949200 chr11:63949189-63949198 chr11:63949188-63949197 chr11:63949189-63949198
32	FOXP2	chr11:63949013-63949358	PFSK-1	brain:	n/a	n/a
33	PML	chr11:63948835-63949537	GM12878	blood:	n/a	n/a
34	EP300	chr11:63949030-63949184	HepG2	liver:	n/a	n/a
35	RUNX3	chr11:63948940-63949434	GM12878	blood:	n/a	n/a
36	USF1	chr11:63948930-63949462	A549	lung:	n/a	chr11:63949187-63949200 chr11:63949189-63949198 chr11:63949187-63949198 chr11:63949188-63949197 chr11:63949189-63949198
37	USF2	chr11:63949000-63949506	K562	blood:	n/a	chr11:63949187-63949200 chr11:63949189-63949198 chr11:63949188-63949197 chr11:63949187-63949198 chr11:63949189-63949198
38	MAX	chr11:63949002-63949356	HepG2	liver:	n/a	chr11:63949189-63949198 chr11:63949189-63949198 chr11:63949187-63949200
39	MXI1	chr11:63948985-63949330	Hela-S3	cervix:	n/a	n/a
40	JUN	chr11:63948963-63949439	K562	blood:	n/a	chr11:63949047-63949057 chr11:63949047-63949057 chr11:63949047-63949057
41	BCL3	chr11:63948843-63949545	A549	lung:	n/a	n/a
42	POLR2A	chr11:63948958-63949428	HUVEC	blood vessel:	n/a	n/a
43	TCF12	chr11:63948841-63949489	A549	lung:	n/a	n/a
44	POLR2A	chr11:63948868-63949452	MCF-7	breast:	n/a	n/a
45	USF1	chr11:63948979-63949389	HepG2	liver:	n/a	chr11:63949187-63949200 chr11:63949189-63949198 chr11:63949187-63949198 chr11:63949188-63949197 chr11:63949189-63949198
46	BHLHE40	chr11:63948921-63949428	K562	blood:	n/a	chr11:63949187-63949200 chr11:63949189-63949198 chr11:63949188-63949197 chr11:63949189-63949198
47	TAF1	chr11:63948988-63949243	H1-hESC	embryonic stem cell:	n/a	n/a
48	REST	chr11:63948912-63949420	SK-N-SH	brain:	n/a	n/a
49	HEY1	chr11:63948971-63949515	HepG2	liver:	n/a	n/a
50	POLR2A	chr11:63947977-63949668	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:63929801..63939249-chr11:63945151..63958671,77	MCF-7	breast:
2	chr11:63927314..63929406-chr11:63948232..63951130,3	K562	blood:
3	chr11:63948212..63950691-chr11:64013231..64015499,3	MCF-7	breast:
4	chr11:63929784..63936274-chr11:63944807..63955078,25	K562	blood:
5	chr11:63929784..63936174-chr11:63947045..63954638,30	K562	blood:
6	chr11:63779445..63782328-chr11:63947827..63950114,2	K562	blood:
7	chr11:63931311..63936745-chr11:63945647..63958123,49	MCF-7	breast:
8	chr11:63948984..63950916-chr11:64036661..64039076,2	MCF-7	breast:
9	chr11:63947888..63950001-chr11:63962324..63964689,2	K562	blood:
10	chr11:63943658..63945912-chr11:63947047..63949667,3	K562	blood:
11	chr11:63937845..63939511-chr11:63948903..63950480,2	K562	blood:

Variant related genes	Relation type
STIP1	TF binding region
ENSG00000256940	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000173457	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000133315	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11601522	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11603042	0.88[CHB][hapmap];0.94[CHD][hapmap];0.83[GIH][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.93[YRI][hapmap];0.81[EUR][1000 genomes]
rs11603192	1.00[ASW][hapmap];0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.93[TSI][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11603538	0.92[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11604782	1.00[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12418535	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12420070	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12787945	0.87[CHD][hapmap]
rs1860368	0.92[CEU][hapmap];0.95[CHD][hapmap];0.94[JPT][hapmap];0.91[MEX][hapmap];0.92[TSI][hapmap];0.92[EUR][1000 genomes]
rs2236648	0.82[CHD][hapmap]
rs2282491	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2282492	1.00[ASW][hapmap];0.88[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];0.94[JPT][hapmap];0.96[MEX][hapmap];0.85[TSI][hapmap];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2429455	0.92[CEU][hapmap];0.83[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.91[MEX][hapmap];0.92[TSI][hapmap];0.91[EUR][1000 genomes]
rs2515241	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2845597	0.92[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3741404	0.88[YRI][hapmap];0.83[EUR][1000 genomes]
rs3888316	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4980508	0.85[CHD][hapmap]
rs594461	0.80[CEU][hapmap]
rs594942	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.88[GIH][hapmap];0.88[JPT][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs595880	0.83[EUR][1000 genomes]
rs604203	0.83[CHB][hapmap];0.97[CHD][hapmap];0.80[JPT][hapmap];0.86[YRI][hapmap]
rs60452247	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs638227	0.80[CEU][hapmap]
rs640999	0.80[CEU][hapmap]
rs641430	0.80[CEU][hapmap]
rs651855	0.80[CEU][hapmap]
rs6591836	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7102177	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7111753	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7112960	1.00[ASW][hapmap];0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.90[TSI][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS 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	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv832185	chr11:63819946-63963532	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	89 gene(s)	inside rSNPs	diseases
6	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
7	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription 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	231 gene(s)	inside rSNPs	diseases
8	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
9	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
10	nsv897663	chr11:63910153-63962152	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	86 gene(s)	inside rSNPs	n/a
11	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
12	nsv468592	chr11:63924446-64042997	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
13	nsv555184	chr11:63924446-64042997	Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
14	nsv897665	chr11:63927695-64026144	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
15	nsv897666	chr11:63929493-64026144	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
16	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
17	nsv468593	chr11:63941734-64089874	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
18	nsv555185	chr11:63941734-64089874	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
19	nsv555186	chr11:63949095-64097233	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs11603384	TRPT1	cis	Heart Left Ventricle	GTEx
rs11603384	MRPL49	cis	cerebellum	SCAN
rs11603384	PRDX5	cis	parietal	SCAN
rs11603384	PPP1R14B	cis	Muscle Skeletal	GTEx
rs11603384	TRPT1	cis	Liver	GTEx
rs11603384	FKBP2	cis	parietal	SCAN
rs11603384	TRMT112	cis	parietal	SCAN
rs11603384	FAU	cis	parietal	SCAN
rs11603384	TRPT1	cis	Muscle Skeletal	GTEx
rs11603384	FKBP2	cis	cerebellum	SCAN
rs11603384	NUDT22	Cis_1M	lymphoblastoid	RTeQTL
rs11603384	TRPT1	cis	multi-tissue	Pritchard

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63934200-63950800	Weak transcription	Gastric	stomach
2	chr11:63943600-63951000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:63944800-63950600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr11:63945000-63952000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr11:63947400-63950000	Enhancers	Psoas Muscle	Psoas
6	chr11:63947600-63952200	Weak transcription	Primary T cells from cord blood	blood
7	chr11:63947800-63949400	Enhancers	Brain Germinal Matrix	brain
8	chr11:63948000-63949200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:63948000-63949600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr11:63948000-63949600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:63948000-63949600	Enhancers	Duodenum Mucosa	Duodenum
12	chr11:63948000-63949600	Enhancers	Left Ventricle	heart
13	chr11:63948000-63949600	Enhancers	Right Atrium	heart
14	chr11:63948000-63949600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
15	chr11:63948000-63949600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
16	chr11:63948000-63949600	Flanking Active TSS	HSMMtube	muscle
17	chr11:63948000-63949800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr11:63948000-63949800	Enhancers	Placenta	Placenta
19	chr11:63948000-63949800	Enhancers	Fetal Stomach	stomach
20	chr11:63948000-63952000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr11:63948000-63952200	Enhancers	Pancreas	Pancrea
22	chr11:63948200-63949200	Genic enhancers	Fetal Intestine Small	intestine
23	chr11:63948200-63949200	Flanking Active TSS	Fetal Muscle Trunk	muscle
24	chr11:63948200-63949400	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr11:63948200-63949600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr11:63948200-63949600	Enhancers	Primary T cells fromperipheralblood	blood
27	chr11:63948200-63949600	Enhancers	Muscle Satellite Cultured Cells	--
28	chr11:63948200-63949600	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr11:63948200-63949600	Enhancers	Colonic Mucosa	Colon
30	chr11:63948200-63949600	Enhancers	Esophagus	oesophagus
31	chr11:63948200-63949600	Enhancers	Placenta Amnion	Placenta Amnion
32	chr11:63948200-63949600	Enhancers	Stomach Mucosa	stomach
33	chr11:63948200-63949800	Enhancers	Fetal Thymus	thymus
34	chr11:63948200-63949800	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr11:63948200-63951400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr11:63948200-63952000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr11:63948400-63949200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr11:63948400-63949200	Flanking Active TSS	Colon Smooth Muscle	Colon
39	chr11:63948400-63949200	Flanking Active TSS	Fetal Heart	heart
40	chr11:63948400-63949200	Flanking Active TSS	Fetal Muscle Leg	muscle
41	chr11:63948400-63949400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr11:63948400-63949400	Enhancers	Fetal Brain Female	brain
43	chr11:63948400-63949600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr11:63948400-63949600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr11:63948400-63949600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr11:63948400-63949600	Flanking Active TSS	Brain Hippocampus Middle	brain
47	chr11:63948400-63949600	Enhancers	Fetal Kidney	kidney
48	chr11:63948400-63949600	Enhancers	Spleen	Spleen
49	chr11:63948400-63949800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr11:63948400-63949800	Enhancers	Fetal Intestine Large	intestine

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