Variant report

Variant	rs1872772
Chromosome Location	chr11:63655846-63655847
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	MXI1	chr11:63655731-63656516	HepG2	liver:	n/a	n/a
2	TCF12	chr11:63655712-63656038	GM12878	blood:	n/a	chr11:63655904-63655911
3	MAZ	chr11:63655557-63656463	K562	blood:	n/a	n/a
4	POLR2A	chr11:63655764-63656149	HCT-116	colon:	n/a	n/a
5	STAT3	chr11:63655846-63656332	MCF10A-Er-Src	breast:	n/a	chr11:63655957-63655969 chr11:63655963-63655975 chr11:63656213-63656221 chr11:63655965-63655977 chr11:63655970-63655982 chr11:63656033-63656045
6	POLR2A	chr11:63655701-63656298	GM18951	blood:	n/a	n/a
7	GABPA	chr11:63655661-63656213	K562	blood:	n/a	n/a
8	TBL1XR1	chr11:63655632-63656088	K562	blood:	n/a	n/a
9	RAD21	chr11:63655804-63656320	H1-hESC	embryonic stem cell:	n/a	chr11:63656100-63656114
10	SIN3AK20	chr11:63655693-63656048	H1-hESC	embryonic stem cell:	n/a	n/a
11	ZNF143	chr11:63655743-63656154	K562	blood:	n/a	chr11:63655958-63655976
12	ELF1	chr11:63655539-63656418	K562	blood:	n/a	chr11:63655949-63655960 chr11:63655948-63655961 chr11:63655949-63655960 chr11:63656304-63656316 chr11:63655950-63655959
13	ELF1	chr11:63655660-63656190	MCF-7	breast:	n/a	chr11:63655949-63655960 chr11:63655948-63655961 chr11:63655949-63655960 chr11:63655950-63655959
14	ELF1	chr11:63655598-63656305	MCF-7	breast:	n/a	chr11:63655949-63655960 chr11:63655948-63655961 chr11:63655949-63655960 chr11:63655950-63655959
15	FOS	chr11:63655597-63655864	MCF10A-Er-Src	breast:	n/a	chr11:63655769-63655777
16	ETS1	chr11:63655637-63656145	K562	blood:	n/a	chr11:63655949-63655958 chr11:63656087-63656098 chr11:63655947-63655958 chr11:63655949-63655958 chr11:63655947-63655957 chr11:63655961-63655972 chr11:63655967-63655978
17	EGR1	chr11:63655589-63655911	K562	blood:	n/a	chr11:63655714-63655727 chr11:63655713-63655728
18	HCFC1	chr11:63655640-63656287	K562	blood:	n/a	n/a
19	SIN3AK20	chr11:63655691-63656147	K562	blood:	n/a	n/a
20	ELF1	chr11:63655810-63656369	HepG2	liver:	n/a	chr11:63655949-63655960 chr11:63655948-63655961 chr11:63655949-63655960 chr11:63656304-63656316 chr11:63655950-63655959
21	TAF1	chr11:63655700-63656241	K562	blood:	n/a	n/a
22	MTA3	chr11:63655648-63656189	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:63655745-63656392	GM12892	blood:	n/a	n/a
24	JUND	chr11:63655571-63656278	K562	blood:	n/a	chr11:63655769-63655777
25	SIN3A	chr11:63655617-63656260	H1-hESC	embryonic stem cell:	n/a	n/a
26	EGR1	chr11:63655497-63656399	K562	blood:	n/a	chr11:63655714-63655727 chr11:63655949-63655958 chr11:63655713-63655728 chr11:63655964-63655977
27	MAFK	chr11:63655617-63655892	IMR90	lung:	n/a	chr11:63655754-63655770 chr11:63655701-63655716 chr11:63655759-63655770 chr11:63655759-63655770
28	ELF1	chr11:63655603-63656452	GM12878	blood:	n/a	chr11:63655949-63655960 chr11:63655948-63655961 chr11:63655949-63655960 chr11:63656304-63656316 chr11:63655950-63655959
29	TCF3	chr11:63655780-63655972	GM12878	blood:	n/a	chr11:63655838-63655851
30	BHLHE40	chr11:63655734-63656380	K562	blood:	n/a	n/a
31	MAZ	chr11:63655608-63656174	GM12878	blood:	n/a	n/a
32	ZNF384	chr11:63655777-63656137	K562	blood:	n/a	n/a
33	SPI1	chr11:63655413-63656438	HL-60	blood:	n/a	n/a
34	MAX	chr11:63655530-63656466	K562	blood:	n/a	n/a
35	CTCF	chr11:63655820-63655970	GM12873	blood:	n/a	n/a
36	MAX	chr11:63655633-63655901	K562	blood:	n/a	n/a
37	POLR2A	chr11:63655577-63656426	K562	blood:	n/a	n/a
38	POLR2A	chr11:63655690-63656314	K562	blood:	n/a	n/a
39	POLR2A	chr11:63655645-63656288	GM12892	blood:	n/a	n/a
40	CHD2	chr11:63655841-63656197	H1-hESC	embryonic stem cell:	n/a	chr11:63655962-63655972
41	POLR2A	chr11:63655822-63656330	MCF-7	breast:	n/a	n/a
42	NR2F2	chr11:63655638-63656163	K562	blood:	n/a	n/a
43	SIN3AK20	chr11:63655802-63656441	HepG2	liver:	n/a	n/a
44	NFIC	chr11:63655814-63656312	HepG2	liver:	n/a	n/a
45	POLR2A	chr11:63655674-63657151	MCF10A-Er-Src	breast:	n/a	n/a
46	ZBTB7A	chr11:63655617-63656153	K562	blood:	n/a	n/a
47	EP300	chr11:63655727-63655874	GM12878	blood:	n/a	n/a
48	POLR2A	chr11:63655032-63656617	HepG2	liver:	n/a	n/a
49	POLR2A	chr11:63655730-63656342	K562	blood:	n/a	n/a
50	MAX	chr11:63654901-63656419	NB4	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:63580299..63582440-chr11:63655697..63658299,3	K562	blood:
2	chr11:63655390..63658583-chr11:63705235..63708313,3	K562	blood:
3	chr11:63654599..63657425-chr11:63952225..63954812,2	K562	blood:
4	chr11:63653210..63656003-chr11:63665435..63667701,2	MCF-7	breast:
5	chr11:63604628..63605373-chr11:63655293..63655881,2	K562	blood:
6	chr11:63581060..63583015-chr11:63654229..63655873,2	MCF-7	breast:
7	chr11:63655513..63657526-chr11:63661698..63663347,2	MCF-7	breast:
8	chr11:63655788..63657631-chr11:63684271..63685886,2	K562	blood:

Variant related genes	Relation type
MARK2	TF binding region
ENSG00000168005	Chromatin interaction
ENSG00000110583	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000167771	Chromatin interaction
ENSG00000072518	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10736731	0.94[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];0.98[TSI][hapmap];0.89[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10751001	0.83[ASN][1000 genomes]
rs10792421	1.00[CEU][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.94[MEX][hapmap];0.98[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10792422	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10792423	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10897452	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10897453	0.82[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.82[GIH][hapmap];0.90[JPT][hapmap];0.82[LWK][hapmap];0.83[MKK][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10897454	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.83[MEX][hapmap];0.83[MKK][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11231600	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11231606	0.84[EUR][1000 genomes]
rs11231624	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11231628	0.86[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11231637	1.00[CEU][hapmap];0.98[GIH][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11231640	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.98[TSI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11231646	0.80[CHB][hapmap]
rs11605500	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12277481	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12576275	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1486936	1.00[CEU][hapmap];0.98[GIH][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2840079	0.89[CEU][hapmap];0.82[CHB][hapmap];0.85[CHD][hapmap];0.88[GIH][hapmap];0.90[JPT][hapmap];0.94[MEX][hapmap];0.98[TSI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs320109	1.00[CEU][hapmap];0.98[GIH][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3802941	0.94[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.93[LWK][hapmap];0.94[MEX][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3850943	0.83[ASN][1000 genomes]
rs4143327	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4963433	0.83[ASN][1000 genomes]
rs4980503	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4980505	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4980507	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4980528	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4980529	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4980532	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4980533	0.88[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61604723	0.81[EUR][1000 genomes]
rs6421686	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6591825	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.98[TSI][hapmap];0.89[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7102006	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7105288	1.00[CEU][hapmap];0.98[GIH][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7108375	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7110843	0.88[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7118913	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7121067	0.90[EUR][1000 genomes]
rs7937314	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7939351	0.81[EUR][1000 genomes]
rs7944519	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.94[MEX][hapmap];0.83[MKK][hapmap];0.98[TSI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7946503	0.81[EUR][1000 genomes]
rs7948656	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs923247	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs928948	0.86[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription 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 target site	100 gene(s)	inside rSNPs	diseases
2	nsv468589	chr11:63515752-63713239	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv555180	chr11:63515752-63713239	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS 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	39 gene(s)	inside rSNPs	diseases
4	esv1839119	chr11:63615554-63680052	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv468590	chr11:63639881-63783352	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv555181	chr11:63639881-63783352	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs1872772	DPF2	cis	parietal	SCAN
rs1872772	SLC22A11	cis	cerebellum	SCAN
rs1872772	ZBTB3	cis	parietal	SCAN
rs1872772	NAALADL1	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63650800-63656000	Weak transcription	Brain Germinal Matrix	brain
2	chr11:63650800-63657600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:63652000-63659600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr11:63652200-63659400	Weak transcription	Fetal Brain Female	brain
5	chr11:63653800-63656000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:63653800-63656000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:63654200-63656000	Enhancers	Brain Hippocampus Middle	brain
8	chr11:63654200-63656000	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr11:63654200-63656400	Enhancers	A549	lung
10	chr11:63654200-63658000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr11:63654200-63658400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr11:63654400-63656000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:63654400-63656000	Enhancers	Colon Smooth Muscle	Colon
14	chr11:63654400-63656000	Enhancers	Fetal Heart	heart
15	chr11:63654400-63656200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr11:63654400-63656200	Enhancers	Primary hematopoietic stem cells	blood
17	chr11:63654400-63656200	Enhancers	Spleen	Spleen
18	chr11:63654400-63656400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr11:63654400-63656600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr11:63654400-63656800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr11:63654400-63656800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr11:63654400-63656800	Enhancers	Psoas Muscle	Psoas
23	chr11:63654400-63657200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr11:63654400-63657200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr11:63654400-63657200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr11:63654400-63657800	Enhancers	Brain Substantia Nigra	brain
27	chr11:63654400-63658200	Enhancers	Lung	lung
28	chr11:63654400-63659000	Enhancers	Brain Angular Gyrus	brain
29	chr11:63654600-63656000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr11:63654600-63656000	Enhancers	Fetal Muscle Leg	muscle
31	chr11:63654600-63656000	Enhancers	Placenta	Placenta
32	chr11:63654600-63656000	Enhancers	Fetal Stomach	stomach
33	chr11:63654600-63656000	Enhancers	Gastric	stomach
34	chr11:63654600-63656000	Enhancers	Right Atrium	heart
35	chr11:63654600-63656000	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr11:63654600-63656800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr11:63654600-63657600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr11:63654800-63656000	Enhancers	Brain Anterior Caudate	brain
39	chr11:63654800-63656200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr11:63654800-63656200	Enhancers	NHLF	lung
41	chr11:63654800-63656400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr11:63654800-63656400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr11:63654800-63656600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr11:63654800-63656800	Enhancers	Fetal Lung	lung
45	chr11:63654800-63657200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
46	chr11:63654800-63664000	Weak transcription	Fetal Brain Male	brain
47	chr11:63655000-63656000	Enhancers	Placenta Amnion	Placenta Amnion
48	chr11:63655000-63656200	Enhancers	Hela-S3	cervix
49	chr11:63655000-63656200	Enhancers	NH-A	brain
50	chr11:63655000-63656400	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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