Variant report

Variant	rs2666562
Chromosome Location	chr11:64405409-64405410
allele	A/C
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	REST	chr11:64405104-64405506	PFSK-1	brain:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
2	REST	chr11:64405216-64405490	PANC-1	pancreas:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
3	YY1	chr11:64405256-64405731	SK-N-SH_RA	brain:	n/a	chr11:64405526-64405535 chr11:64405515-64405537 chr11:64405525-64405537 chr11:64405612-64405621 chr11:64405527-64405537
4	REST	chr11:64405131-64405526	HCT-116	colon:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
5	REST	chr11:64405110-64405483	HL-60	blood:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
6	REST	chr11:64405147-64405435	SK-N-SH	brain:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
7	REST	chr11:64405024-64405526	H1-hESC	embryonic stem cell:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
8	REST	chr11:64405133-64405523	HCT-116	colon:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
9	CTBP2	chr11:64405252-64405880	H1-hESC	embryonic stem cell:	n/a	n/a
10	REST	chr11:64405044-64405551	PANC-1	pancreas:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
11	REST	chr11:64405175-64405492	PANC-1	pancreas:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
12	POLR2A	chr11:64405241-64406197	H1-neurons	neurons:	n/a	n/a
13	SIN3A	chr11:64405175-64405771	H1-hESC	embryonic stem cell:	n/a	chr11:64405311-64405321
14	REST	chr11:64405063-64405535	H1-hESC	embryonic stem cell:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
15	REST	chr11:64405169-64405784	SK-N-SH	brain:	n/a	chr11:64405566-64405579 chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
16	REST	chr11:64404994-64405562	HL-60	blood:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
17	REST	chr11:64405193-64405465	K562	blood:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
18	REST	chr11:64405218-64405458	HepG2	liver:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
19	GABPA	chr11:64405306-64405712	H1-hESC	embryonic stem cell:	n/a	chr11:64405612-64405621
20	REST	chr11:64404970-64405552	ECC-1	luminal epithelium:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
21	ZNF143	chr11:64405183-64405466	H1-hESC	embryonic stem cell:	n/a	n/a
22	REST	chr11:64405109-64405419	MCF-7	breast:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
23	MAX	chr11:64405231-64405792	H1-hESC	embryonic stem cell:	n/a	n/a
24	REST	chr11:64405086-64405519	U87	brain:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
25	YY1	chr11:64405345-64405706	H1-hESC	embryonic stem cell:	n/a	chr11:64405526-64405535 chr11:64405515-64405537 chr11:64405525-64405537 chr11:64405612-64405621 chr11:64405527-64405537
26	REST	chr11:64404976-64405662	ECC-1	luminal epithelium:	n/a	chr11:64405566-64405579 chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
27	REST	chr11:64405070-64405560	SK-N-SH	brain:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
28	REST	chr11:64405038-64405525	A549	lung:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
29	YY1	chr11:64405259-64405878	SK-N-SH_RA	brain:	n/a	chr11:64405526-64405535 chr11:64405515-64405537 chr11:64405525-64405537 chr11:64405612-64405621 chr11:64405527-64405537
30	REST	chr11:64405037-64406070	H1-neurons	neurons:	n/a	chr11:64405898-64405911 chr11:64405566-64405579 chr11:64405985-64405998 chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405856-64405866 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
31	REST	chr11:64405074-64405505	PFSK-1	brain:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
32	SIN3AK20	chr11:64405157-64405534	H1-hESC	embryonic stem cell:	n/a	n/a
33	YY1	chr11:64405245-64406156	H1-hESC	embryonic stem cell:	n/a	chr11:64405526-64405535 chr11:64405938-64405949 chr11:64405515-64405537 chr11:64405525-64405537 chr11:64405612-64405621 chr11:64405527-64405537
34	REST	chr11:64405078-64405553	MCF-7	breast:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
35	JUND	chr11:64405234-64405670	H1-hESC	embryonic stem cell:	n/a	n/a
36	MXI1	chr11:64404615-64406843	SK-N-SH	brain:	n/a	chr11:64404976-64404991 chr11:64404974-64404989
37	POLR2A	chr11:64405383-64406092	H1-neurons	neurons:	n/a	n/a
38	REST	chr11:64405072-64405503	PANC-1	pancreas:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
39	REST	chr11:64405083-64405466	GM12878	blood:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325
40	CTCF	chr11:64405400-64405550	SK-N-SH_RA	brain:	n/a	n/a
41	REST	chr11:64405162-64405455	A549	lung:	n/a	chr11:64405305-64405325 chr11:64405305-64405325 chr11:64405311-64405320 chr11:64405316-64405325 chr11:64405306-64405324 chr11:64405305-64405325

No.	Distal block	Cell Line	Cell type	Cell Stage
1	11:64187725-64189071..11:64402707-64415880	K562	blood:

Variant related genes	Relation type
NRXN2	TF binding region
ENSG00000231492	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10466694	1.00[EUR][1000 genomes]
rs11231806	1.00[EUR][1000 genomes]
rs11231811	1.00[EUR][1000 genomes]
rs11231812	1.00[EUR][1000 genomes]
rs11231865	1.00[EUR][1000 genomes]
rs11231866	1.00[EUR][1000 genomes]
rs11821081	1.00[EUR][1000 genomes]
rs1212539	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1212851	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12273948	1.00[EUR][1000 genomes]
rs12281931	1.00[EUR][1000 genomes]
rs12293573	1.00[EUR][1000 genomes]
rs17146100	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17146110	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17146119	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs1787671	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2022049	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2518908	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2666561	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2904961	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2959651	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3016758	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs3016759	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41323046	1.00[EUR][1000 genomes]
rs475704	1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs512926	0.92[YRI][hapmap];1.00[EUR][1000 genomes]
rs516041	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs534052	1.00[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs534073	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs535606	1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs541305	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs545167	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs545819	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs546323	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs550930	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs553618	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs559095	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs559977	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56186064	1.00[EUR][1000 genomes]
rs565688	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs573545	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57371796	1.00[EUR][1000 genomes]
rs579175	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58571986	1.00[EUR][1000 genomes]
rs6591863	1.00[EUR][1000 genomes]
rs7110778	1.00[EUR][1000 genomes]
rs7113097	1.00[EUR][1000 genomes]
rs7127435	1.00[EUR][1000 genomes]
rs73492134	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73492139	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73492140	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73492144	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73494206	1.00[EUR][1000 genomes]
rs7948607	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7948832	1.00[EUR][1000 genomes]
rs9326433	1.00[EUR][1000 genomes]
rs9326434	1.00[EUR][1000 genomes]
rs9666331	1.00[EUR][1000 genomes]
rs9666856	1.00[EUR][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	nsv897693	chr11:64305452-64440920	Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv2422214	chr11:64312491-64483418	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv832188	chr11:64315368-64485209	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv468596	chr11:64334114-64527080	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv555195	chr11:64334114-64527080	Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv897694	chr11:64334114-64584959	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
7	nsv818842	chr11:64345448-64546391	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
8	nsv528506	chr11:64345448-64701030	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
9	nsv555196	chr11:64357072-64559898	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
10	nsv897695	chr11:64357072-64701030	Weak transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
11	nsv897696	chr11:64365796-64412877	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1051350	chr11:64372906-64533632	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
13	nsv555198	chr11:64373899-64573589	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
14	esv1804443	chr11:64386453-64534785	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
15	nsv555199	chr11:64394684-64408646	Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64397400-64406000	Weak transcription	NHDF-Ad	bronchial
2	chr11:64400200-64408200	Weak transcription	HSMM	muscle
3	chr11:64401800-64405800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr11:64402600-64405800	Weak transcription	HSMMtube	muscle
5	chr11:64403000-64410400	Weak transcription	Aorta	Aorta
6	chr11:64403200-64407400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr11:64403400-64407000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr11:64403400-64407800	Weak transcription	Osteobl	bone
9	chr11:64404200-64406400	Enhancers	Brain Substantia Nigra	brain
10	chr11:64404400-64405600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:64404400-64405600	Bivalent Enhancer	Fetal Muscle Leg	muscle
12	chr11:64404400-64406600	Enhancers	Primary B cells from peripheral blood	blood
13	chr11:64404800-64406200	Bivalent Enhancer	Placenta	Placenta
14	chr11:64404800-64406400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr11:64405000-64405600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:64405000-64405600	Enhancers	Primary B cells from cord blood	blood
17	chr11:64405000-64405600	Bivalent Enhancer	Fetal Thymus	thymus
18	chr11:64405000-64405600	Flanking Active TSS	Rectal Smooth Muscle	rectum
19	chr11:64405000-64405800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:64405000-64405800	Enhancers	Fetal Lung	lung
21	chr11:64405000-64406200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
22	chr11:64405000-64406400	Active TSS	Brain Angular Gyrus	brain
23	chr11:64405200-64405600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
24	chr11:64405200-64405600	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr11:64405200-64405600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
26	chr11:64405200-64405600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
27	chr11:64405200-64405600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr11:64405200-64405600	Bivalent Enhancer	Esophagus	oesophagus
29	chr11:64405200-64405600	Flanking Active TSS	Fetal Intestine Large	intestine
30	chr11:64405200-64405600	Flanking Active TSS	Fetal Intestine Small	intestine
31	chr11:64405200-64405600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
32	chr11:64405200-64405600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
33	chr11:64405200-64405600	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr11:64405200-64405800	Bivalent Enhancer	Adipose Nuclei	Adipose
35	chr11:64405200-64405800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
36	chr11:64405200-64406000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
37	chr11:64405200-64406000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
38	chr11:64405200-64406000	Active TSS	Brain Anterior Caudate	brain
39	chr11:64405200-64406000	Flanking Active TSS	Colonic Mucosa	Colon
40	chr11:64405200-64406000	Active TSS	Fetal Kidney	kidney
41	chr11:64405200-64406000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
42	chr11:64405200-64406000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
43	chr11:64405200-64406200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr11:64405200-64406200	Active TSS	H9 Cell Line	embryonic stem cell
45	chr11:64405200-64406200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
46	chr11:64405200-64406400	Flanking Active TSS	Fetal Brain Male	brain
47	chr11:64405200-64408000	Enhancers	Spleen	Spleen
48	chr11:64405400-64405600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:64405400-64405600	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr11:64405400-64405600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell

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