Variant report

Variant	rs3759056
Chromosome Location	chr11:64126050-64126051
allele	C/T
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	HCFC1	chr11:64124546-64127782	Hela-S3	cervix:	n/a	n/a
2	SMARCB1	chr11:64125210-64127144	Hela-S3	cervix:	n/a	n/a
3	BHLHE40	chr11:64125554-64126887	HepG2	liver:	n/a	chr11:64126316-64126332 chr11:64126780-64126796 chr11:64126632-64126648 chr11:64126633-64126649
4	POLR2A	chr11:64125688-64127031	GM12892	blood:	n/a	n/a
5	MAX	chr11:64125485-64127208	HepG2	liver:	n/a	chr11:64125961-64125977 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64125725-64125735
6	POLR2A	chr11:64125773-64127153	HepG2	liver:	n/a	n/a
7	POLR2A	chr11:64125316-64127393	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr11:64125414-64126909	GM12878	blood:	n/a	n/a
9	POLR2A	chr11:64125303-64127100	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr11:64125026-64127534	K562	blood:	n/a	n/a
11	POLR2A	chr11:64125487-64126143	GM12892	blood:	n/a	n/a
12	MAX	chr11:64125298-64127158	K562	blood:	n/a	chr11:64125961-64125977 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64125725-64125735
13	MAX	chr11:64125460-64126256	A549	lung:	n/a	chr11:64125961-64125977 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64125725-64125735
14	SMARCC2	chr11:64124862-64126548	Hela-S3	cervix:	n/a	n/a
15	BHLHE40	chr11:64125430-64126924	K562	blood:	n/a	chr11:64126316-64126332 chr11:64126780-64126796 chr11:64126632-64126648 chr11:64126633-64126649
16	MAFK	chr11:64125403-64126052	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr11:64126040-64126190	HEK293	kidney:	n/a	n/a
18	NR2F2	chr11:64125226-64126455	K562	blood:	n/a	n/a
19	MAZ	chr11:64125935-64127589	IMR90	lung:	n/a	chr11:64125961-64125977 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64127233-64127243
20	MXI1	chr11:64125646-64127658	SK-N-SH	brain:	n/a	n/a
21	ZBTB7A	chr11:64125127-64127287	K562	blood:	n/a	n/a
22	POLR2A	chr11:64125206-64126100	K562	blood:	n/a	n/a
23	YY1	chr11:64126034-64127075	K562	blood:	n/a	chr11:64126559-64126573 chr11:64126605-64126619 chr11:64126593-64126607 chr11:64126565-64126579 chr11:64126630-64126644 chr11:64126497-64126511 chr11:64126792-64126803
24	CBX3	chr11:64125256-64126131	K562	blood:	n/a	n/a
25	ZBTB7A	chr11:64125386-64127369	ECC-1	luminal epithelium:	n/a	n/a
26	UBTF	chr11:64126028-64126060	K562	blood:	n/a	n/a
27	MAZ	chr11:64125259-64127214	Hela-S3	cervix:	n/a	chr11:64125961-64125977 chr11:64125278-64125288 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64125274-64125284 chr11:64125725-64125735
28	MAX	chr11:64125327-64127627	A549	lung:	n/a	chr11:64125961-64125977 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64127233-64127243 chr11:64125725-64125735
29	SMARCC1	chr11:64125052-64126564	Hela-S3	cervix:	n/a	n/a
30	E2F6	chr11:64125810-64127040	K562	blood:	n/a	chr11:64127012-64127022
31	REST	chr11:64126020-64127179	H1-neurons	neurons:	n/a	chr11:64126262-64126272 chr11:64126565-64126578 chr11:64127126-64127139 chr11:64126472-64126485 chr11:64126260-64126274
32	SIN3AK20	chr11:64126026-64127677	MCF-7	breast:	n/a	n/a
33	MAX	chr11:64125772-64126096	HepG2	liver:	n/a	chr11:64125961-64125977 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988
34	TFAP2C	chr11:64125325-64126858	Hela-S3	cervix:	n/a	chr11:64126461-64126476
35	POLR2A	chr11:64125369-64128440	HL-60	blood:	n/a	n/a
36	ZBTB7A	chr11:64125314-64127395	ECC-1	luminal epithelium:	n/a	n/a
37	JUN	chr11:64124797-64127116	K562	blood:	n/a	chr11:64125503-64125511
38	TCF12	chr11:64125900-64127247	A549	lung:	n/a	chr11:64126347-64126355
39	MYC	chr11:64125414-64126123	K562	blood:	n/a	chr11:64125961-64125977 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64125725-64125735
40	CTCF	chr11:64126020-64126170	HepG2	liver:	n/a	n/a
41	ZBTB7A	chr11:64125459-64126205	K562	blood:	n/a	n/a
42	MAX	chr11:64125316-64126060	Hela-S3	cervix:	n/a	chr11:64125961-64125977 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64125725-64125735
43	POLR2A	chr11:64125304-64127044	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr11:64125241-64126075	GM12878	blood:	n/a	n/a
45	TEAD4	chr11:64126048-64126898	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64110456..64113002-chr11:64125236..64127679,2	MCF-7	breast:
2	chr11:63972047..63977847-chr11:64122012..64128099,8	K562	blood:
3	chr11:64041009..64043331-chr11:64125161..64128159,2	MCF-7	breast:
4	chr11:64082853..64088243-chr11:64119014..64129028,17	MCF-7	breast:
5	chr11:64070250..64072559-chr11:64125217..64126731,2	MCF-7	breast:
6	chr11:64125330..64128537-chr11:64215213..64218115,3	MCF-7	breast:
7	chr11:64017685..64020898-chr11:64124130..64127721,3	MCF-7	breast:
8	chr11:64000008..64002901-chr11:64125113..64127418,2	MCF-7	breast:
9	chr11:64070986..64076286-chr11:64124810..64128616,7	K562	blood:
10	chr11:64119430..64124364-chr11:64124831..64128743,7	MCF-7	breast:
11	chr11:64013360..64015283-chr11:64125680..64128243,2	MCF-7	breast:
12	chr11:64004012..64005762-chr11:64124323..64126720,2	MCF-7	breast:
13	chr11:64062668..64065011-chr11:64124225..64126837,3	MCF-7	breast:
14	chr11:64124497..64126994-chr11:64509396..64512374,2	K562	blood:
15	chr11:64052659..64056055-chr11:64125689..64127630,3	MCF-7	breast:
16	chr11:64013219..64015249-chr11:64126039..64128658,2	K562	blood:
17	chr11:64008386..64010951-chr11:64125361..64127756,4	MCF-7	breast:
18	chr11:64053151..64055063-chr11:64124109..64127002,2	K562	blood:
19	chr11:64083913..64086967-chr11:64122125..64127376,8	MCF-7	breast:
20	chr11:64125259..64126829-chr11:64127521..64129918,2	MCF-7	breast:
21	chr11:64080620..64083894-chr11:64124180..64128334,3	MCF-7	breast:
22	chr11:64124989..64126699-chr11:64216058..64218143,2	K562	blood:
23	chr11:64124540..64126165-chr11:64416805..64418709,2	MCF-7	breast:

Variant related genes	Relation type
RPS6KA4	TF binding region
ENSG00000068831	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000149781	Chromatin interaction
ENSG00000181908	Chromatin interaction
ENSG00000207024	Chromatin interaction
ENSG00000110011	Chromatin interaction
ENSG00000182450	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000173511	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000256940	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000256116	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000173486	Chromatin interaction
ENSG00000149782	Chromatin interaction
ENSG00000173457	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10128595	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10128649	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10556	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10732887	0.87[ASN][1000 genomes]
rs1207462	0.89[ASN][1000 genomes]
rs1213140	0.91[ASN][1000 genomes]
rs12271952	0.86[ASN][1000 genomes]
rs12281471	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12283639	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12287065	0.93[ASN][1000 genomes]
rs12574188	0.89[ASN][1000 genomes]
rs12575515	0.89[ASN][1000 genomes]
rs12575690	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12577422	0.87[ASN][1000 genomes]
rs12577425	0.85[ASN][1000 genomes]
rs1468558	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17159027	1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1783518	0.87[ASN][1000 genomes]
rs2079786	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2232410	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2232417	1.00[EUR][1000 genomes]
rs2282548	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2286612	0.84[ASN][1000 genomes]
rs2289572	0.98[ASN][1000 genomes]
rs2302262	0.93[ASN][1000 genomes]
rs28682946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41294376	0.89[ASN][1000 genomes]
rs41294424	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs473379	0.89[ASN][1000 genomes]
rs474430	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs490720	0.89[ASN][1000 genomes]
rs4930167	0.87[ASN][1000 genomes]
rs493052	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs494998	0.89[ASN][1000 genomes]
rs518698	0.87[ASN][1000 genomes]
rs520277	0.87[ASN][1000 genomes]
rs539008	0.89[ASN][1000 genomes]
rs539250	0.87[ASN][1000 genomes]
rs543767	0.83[ASN][1000 genomes]
rs554812	0.89[ASN][1000 genomes]
rs569741	0.89[ASN][1000 genomes]
rs575081	0.89[ASN][1000 genomes]
rs58010797	0.87[ASN][1000 genomes]
rs58488481	0.89[ASN][1000 genomes]
rs58721876	0.93[ASN][1000 genomes]
rs59283629	0.93[ASN][1000 genomes]
rs60421451	0.95[ASN][1000 genomes]
rs60579179	0.87[ASN][1000 genomes]
rs61431997	0.93[ASN][1000 genomes]
rs621816	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs650008	1.00[EUR][1000 genomes]
rs687424	1.00[EUR][1000 genomes]
rs7110262	0.93[ASN][1000 genomes]
rs7121001	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7950922	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7951858	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7952435	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 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	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
6	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
7	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
8	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer 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 miRNA target site	179 gene(s)	inside rSNPs	diseases
9	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' 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	180 gene(s)	inside rSNPs	diseases
10	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
11	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
12	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
13	nsv1043277	chr11:64002997-64132030	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
14	nsv897685	chr11:64048912-64150370	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
15	nsv818841	chr11:64097233-64129722	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
16	nsv897688	chr11:64107735-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
17	nsv897689	chr11:64109118-64148420	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
18	nsv897690	chr11:64118422-64135298	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
19	nsv897691	chr11:64118422-64137875	Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
20	nsv832187	chr11:64121969-64312300	Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' 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	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64123200-64126200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:64123800-64126200	Enhancers	Pancreas	Pancrea
3	chr11:64124000-64126200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:64124200-64126200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr11:64124200-64126200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr11:64124200-64126200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:64124200-64126400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr11:64124400-64126200	Enhancers	Placenta Amnion	Placenta Amnion
9	chr11:64124800-64126600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr11:64125000-64126200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:64125000-64126200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr11:64125000-64126200	Enhancers	Gastric	stomach
13	chr11:64125000-64126200	Enhancers	Lung	lung
14	chr11:64125000-64126200	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr11:64125200-64126200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr11:64125200-64126200	Enhancers	Primary B cells from cord blood	blood
17	chr11:64125200-64126200	Enhancers	Small Intestine	intestine
18	chr11:64125200-64126200	Enhancers	NH-A	brain
19	chr11:64125200-64126400	Flanking Active TSS	A549	lung
20	chr11:64125200-64126400	Flanking Active TSS	Hela-S3	cervix
21	chr11:64125200-64126400	Flanking Active TSS	K562	blood
22	chr11:64125400-64126200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:64125400-64126200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr11:64125400-64126200	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr11:64125400-64126200	Enhancers	Primary hematopoietic stem cells	blood
26	chr11:64125400-64126200	Enhancers	Ovary	ovary
27	chr11:64125400-64126200	Enhancers	Spleen	Spleen
28	chr11:64125400-64126400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr11:64125400-64126400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr11:64125400-64126400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr11:64125400-64126400	Flanking Active TSS	Duodenum Mucosa	Duodenum
32	chr11:64125400-64126400	Flanking Active TSS	Dnd41	blood
33	chr11:64125600-64126200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr11:64125600-64126200	Enhancers	Primary B cells from peripheral blood	blood
35	chr11:64125600-64126200	Enhancers	Thymus	Thymus
36	chr11:64125600-64126200	Enhancers	HSMMtube	muscle
37	chr11:64125600-64126400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr11:64125600-64126400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr11:64125600-64126400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr11:64125600-64126400	Flanking Active TSS	Colonic Mucosa	Colon
41	chr11:64125600-64126400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr11:64125600-64126400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
43	chr11:64125600-64126600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr11:64125600-64126600	Flanking Active TSS	NHEK	skin
45	chr11:64125600-64127800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr11:64125800-64126200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr11:64125800-64126200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:64125800-64126200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr11:64125800-64126200	Flanking Active TSS	Rectal Smooth Muscle	rectum
50	chr11:64125800-64126200	Flanking Bivalent TSS/Enh	HepG2	liver

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