Variant report

Variant	rs562831674
Chromosome Location	chr11:71497528-71497529
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	PAX5	chr11:71497526-71498896	GM12878	blood:	n/a	chr11:71498296-71498315 chr11:71497959-71497978
2	TAF1	chr11:71497138-71499373	HepG2	liver:	n/a	n/a
3	JUND	chr11:71497038-71498140	HepG2	liver:	n/a	chr11:71497963-71497972 chr11:71497105-71497114 chr11:71497863-71497872
4	FOSL2	chr11:71496807-71499766	HepG2	liver:	n/a	chr11:71497963-71497972 chr11:71499319-71499327 chr11:71497105-71497114 chr11:71499317-71499329 chr11:71497863-71497872
5	MYBL2	chr11:71497308-71497784	HepG2	liver:	n/a	n/a
6	SP1	chr11:71497067-71499393	GM12878	blood:	n/a	chr11:71497633-71497642 chr11:71497981-71497993 chr11:71498074-71498086 chr11:71497909-71497921 chr11:71498075-71498084 chr11:71497104-71497113 chr11:71498111-71498123 chr11:71498112-71498122 chr11:71498568-71498580 chr11:71498112-71498121 chr11:71497960-71497972 chr11:71497601-71497615 chr11:71498076-71498085 chr11:71498298-71498307 chr11:71497961-71497970 chr11:71498230-71498244 chr11:71498230-71498239 chr11:71498229-71498241 chr11:71497981-71497993 chr11:71498569-71498579 chr11:71497600-71497612 chr11:71498111-71498123 chr11:71497961-71497975 chr11:71498074-71498086 chr11:71498297-71498309 chr11:71498113-71498122 chr11:71498569-71498579 chr11:71498569-71498578 chr11:71498063-71498075 chr11:71497102-71497114 chr11:71498212-71498226 chr11:71498112-71498121 chr11:71498063-71498075 chr11:71498231-71498240 chr11:71498299-71498308 chr11:71498075-71498089 chr11:71497600-71497612 chr11:71497602-71497611 chr11:71498297-71498309 chr11:71497962-71497971 chr11:71497910-71497924 chr11:71497601-71497610 chr11:71497982-71497991 chr11:71497960-71497972 chr11:71498111-71498122 chr11:71498298-71498308 chr11:71497102-71497114 chr11:71497772-71497781 chr11:71498570-71498579 chr11:71498569-71498578 chr11:71498008-71498020 chr11:71498229-71498241 chr11:71498064-71498073 chr11:71498568-71498580 chr11:71498298-71498307
7	POLR2A	chr11:71497480-71498065	PANC-1	pancreas:	n/a	n/a
8	POLR2A	chr11:71497381-71497942	HepG2	liver:	n/a	n/a
9	SP1	chr11:71497346-71498828	A549	lung:	n/a	chr11:71497633-71497642 chr11:71497981-71497993 chr11:71498074-71498086 chr11:71497909-71497921 chr11:71498075-71498084 chr11:71498111-71498123 chr11:71498112-71498122 chr11:71498568-71498580 chr11:71498112-71498121 chr11:71497960-71497972 chr11:71497601-71497615 chr11:71498076-71498085 chr11:71498298-71498307 chr11:71497961-71497970 chr11:71498230-71498244 chr11:71498230-71498239 chr11:71498229-71498241 chr11:71497981-71497993 chr11:71498569-71498579 chr11:71497600-71497612 chr11:71498111-71498123 chr11:71497961-71497975 chr11:71498074-71498086 chr11:71498297-71498309 chr11:71498113-71498122 chr11:71498569-71498579 chr11:71498569-71498578 chr11:71498063-71498075 chr11:71498212-71498226 chr11:71498112-71498121 chr11:71498063-71498075 chr11:71498231-71498240 chr11:71498299-71498308 chr11:71498075-71498089 chr11:71497600-71497612 chr11:71497602-71497611 chr11:71498297-71498309 chr11:71497962-71497971 chr11:71497910-71497924 chr11:71497601-71497610 chr11:71497982-71497991 chr11:71497960-71497972 chr11:71498111-71498122 chr11:71498298-71498308 chr11:71497772-71497781 chr11:71498570-71498579 chr11:71498569-71498578 chr11:71498008-71498020 chr11:71498229-71498241 chr11:71498064-71498073 chr11:71498568-71498580 chr11:71498298-71498307
10	POLR2A	chr11:71497497-71497898	ECC-1	luminal epithelium:	n/a	n/a
11	SP1	chr11:71496342-71498724	HepG2	liver:	n/a	chr11:71497633-71497642 chr11:71497981-71497993 chr11:71498074-71498086 chr11:71497909-71497921 chr11:71498075-71498084 chr11:71497104-71497113 chr11:71498111-71498123 chr11:71498112-71498122 chr11:71498568-71498580 chr11:71498112-71498121 chr11:71497960-71497972 chr11:71497601-71497615 chr11:71498076-71498085 chr11:71498298-71498307 chr11:71497961-71497970 chr11:71498230-71498244 chr11:71498230-71498239 chr11:71498229-71498241 chr11:71497981-71497993 chr11:71498569-71498579 chr11:71497600-71497612 chr11:71498111-71498123 chr11:71497961-71497975 chr11:71498074-71498086 chr11:71498297-71498309 chr11:71498113-71498122 chr11:71498569-71498579 chr11:71498569-71498578 chr11:71498063-71498075 chr11:71497102-71497114 chr11:71498212-71498226 chr11:71498112-71498121 chr11:71498063-71498075 chr11:71498231-71498240 chr11:71498299-71498308 chr11:71498075-71498089 chr11:71497600-71497612 chr11:71497602-71497611 chr11:71498297-71498309 chr11:71497962-71497971 chr11:71497910-71497924 chr11:71497601-71497610 chr11:71497982-71497991 chr11:71497960-71497972 chr11:71498111-71498122 chr11:71498298-71498308 chr11:71497102-71497114 chr11:71497772-71497781 chr11:71498570-71498579 chr11:71498569-71498578 chr11:71498008-71498020 chr11:71498229-71498241 chr11:71498064-71498073 chr11:71498568-71498580 chr11:71498298-71498307
12	SP1	chr11:71497397-71498749	GM12878	blood:	n/a	chr11:71497633-71497642 chr11:71497981-71497993 chr11:71498074-71498086 chr11:71497909-71497921 chr11:71498075-71498084 chr11:71498111-71498123 chr11:71498112-71498122 chr11:71498568-71498580 chr11:71498112-71498121 chr11:71497960-71497972 chr11:71497601-71497615 chr11:71498076-71498085 chr11:71498298-71498307 chr11:71497961-71497970 chr11:71498230-71498244 chr11:71498230-71498239 chr11:71498229-71498241 chr11:71497981-71497993 chr11:71498569-71498579 chr11:71497600-71497612 chr11:71498111-71498123 chr11:71497961-71497975 chr11:71498074-71498086 chr11:71498297-71498309 chr11:71498113-71498122 chr11:71498569-71498579 chr11:71498569-71498578 chr11:71498063-71498075 chr11:71498212-71498226 chr11:71498112-71498121 chr11:71498063-71498075 chr11:71498231-71498240 chr11:71498299-71498308 chr11:71498075-71498089 chr11:71497600-71497612 chr11:71497602-71497611 chr11:71498297-71498309 chr11:71497962-71497971 chr11:71497910-71497924 chr11:71497601-71497610 chr11:71497982-71497991 chr11:71497960-71497972 chr11:71498111-71498122 chr11:71498298-71498308 chr11:71497772-71497781 chr11:71498570-71498579 chr11:71498569-71498578 chr11:71498008-71498020 chr11:71498229-71498241 chr11:71498064-71498073 chr11:71498568-71498580 chr11:71498298-71498307
13	POLR2A	chr11:71497345-71497612	H1-hESC	embryonic stem cell:	n/a	n/a
14	HCFC1	chr11:71497438-71499395	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr11:71497347-71497858	HepG2	liver:	n/a	n/a
16	PAX5	chr11:71496944-71499500	GM12878	blood:	n/a	chr11:71498296-71498315 chr11:71497959-71497978
17	POLR2A	chr11:71497060-71498099	HepG2	liver:	n/a	n/a
18	POLR2A	chr11:71497312-71498032	HepG2	liver:	n/a	n/a
19	MXI1	chr11:71497491-71499616	IMR90	lung:	n/a	n/a
20	TAF1	chr11:71496991-71499421	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr11:71497052-71500345	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr11:71497084-71498404	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr11:71497430-71498081	A549	lung:	n/a	n/a
24	POLR2A	chr11:71496463-71501471	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr11:71497188-71499391	HepG2	liver:	n/a	n/a
26	GATA1	chr11:71497480-71498384	PBDE	blood:	n/a	n/a
27	POLR2A	chr11:71497444-71497933	SK-N-SH	brain:	n/a	n/a
28	POLR2A	chr11:71497508-71498020	K562	blood:	n/a	n/a
29	TCF3	chr11:71497502-71498096	GM12878	blood:	n/a	n/a
30	RXRA	chr11:71497078-71497913	HepG2	liver:	n/a	n/a
31	POLR2A	chr11:71497483-71498008	HUVEC	blood vessel:	n/a	n/a
32	FOXA1	chr11:71496607-71497541	HepG2	liver:	n/a	n/a
33	POLR2A	chr11:71497509-71499394	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr11:71497460-71498073	U87	brain:	n/a	n/a
35	POLR2A	chr11:71497306-71498409	H1-hESC	embryonic stem cell:	n/a	n/a
36	GABPA	chr11:71497415-71498137	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr11:71497497-71497887	ECC-1	luminal epithelium:	n/a	n/a
38	YY1	chr11:71497528-71499051	HepG2	liver:	n/a	chr11:71497600-71497614 chr11:71498570-71498579 chr11:71497960-71497974 chr11:71498682-71498691
39	POLR2A	chr11:71497407-71499883	SK-N-MC	brain:	n/a	n/a
40	HEY1	chr11:71497348-71497960	K562	blood:	n/a	n/a
41	POLR2A	chr11:71497354-71500670	GM12878	blood:	n/a	n/a
42	POLR2A	chr11:71497524-71497856	MCF-7	breast:	n/a	n/a
43	TBP	chr11:71497475-71497809	H1-hESC	embryonic stem cell:	n/a	n/a
44	PAX5	chr11:71497467-71498751	GM12878	blood:	n/a	chr11:71498296-71498315 chr11:71497959-71497978
45	POLR2A	chr11:71497431-71499345	Raji	blood:	n/a	n/a
46	POLR2A	chr11:71497344-71497922	HepG2	liver:	n/a	n/a
47	HEY1	chr11:71496886-71497954	HepG2	liver:	n/a	n/a
48	POLR2A	chr11:71497426-71498004	PFSK-1	brain:	n/a	n/a
49	POLR2A	chr11:71496992-71500721	GM12892	blood:	n/a	n/a
50	SMARCB1	chr11:71497435-71499302	Hela-S3	cervix:	n/a	n/a

Variant related genes	Relation type
FAM86C1	TF binding region

Extended variants
information (count: 34 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
2	nsv1037088	chr11:71293875-71538991	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	esv3527986	chr11:71298409-71620955	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
4	esv3527987	chr11:71298409-71620955	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	nsv1036258	chr11:71299175-71523551	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv1041027	chr11:71299175-71527896	Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv1051879	chr11:71299175-71536860	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
8	nsv1044041	chr11:71299175-71538991	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
9	esv2761682	chr11:71299175-71619923	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
10	nsv897903	chr11:71316093-71523766	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv897904	chr11:71316093-71615727	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
12	nsv1035306	chr11:71326941-71523551	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
13	nsv972041	chr11:71330518-71615123	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
14	esv1808002	chr11:71330564-71522967	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
15	nsv832205	chr11:71336700-71523817	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
16	esv3369013	chr11:71338874-71612242	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
17	nsv1054575	chr11:71352127-71536860	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
18	nsv1047568	chr11:71352127-71538991	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
19	nsv1047177	chr11:71360190-71513585	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv427893	chr11:71363639-71529688	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	esv2758276	chr11:71363639-71657576	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
22	esv2759836	chr11:71363639-71657576	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
23	nsv428262	chr11:71363639-71804055	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
24	nsv1049480	chr11:71363999-71533919	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
25	nsv897905	chr11:71371354-71615727	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
26	esv1819073	chr11:71371742-71618164	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
27	nsv1044072	chr11:71379653-71527699	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
28	nsv1038551	chr11:71379653-71533919	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
29	nsv897906	chr11:71386905-71543708	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
30	nsv897907	chr11:71386905-71549174	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
31	nsv1045511	chr11:71395657-71527896	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
32	nsv1043197	chr11:71423465-71527699	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
33	nsv1037092	chr11:71443870-71527699	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
34	esv3379456	chr11:71496804-71499952	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71496800-71499200	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr11:71497000-71499400	Active TSS	Breast Myoepithelial Primary Cells	Breast
3	chr11:71497200-71497600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:71497200-71497600	Flanking Active TSS	Primary B cells from peripheral blood	blood
5	chr11:71497200-71497600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
6	chr11:71497200-71497600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
7	chr11:71497200-71497600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:71497200-71497600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
9	chr11:71497200-71497600	Flanking Active TSS	Fetal Intestine Small	intestine
10	chr11:71497200-71497600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
11	chr11:71497200-71497600	Enhancers	Stomach Mucosa	stomach
12	chr11:71497200-71497600	Flanking Active TSS	Hela-S3	cervix
13	chr11:71497200-71497800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr11:71497200-71497800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
15	chr11:71497200-71497800	Flanking Active TSS	Adipose Nuclei	Adipose
16	chr11:71497200-71497800	Flanking Active TSS	Fetal Intestine Large	intestine
17	chr11:71497200-71497800	Flanking Active TSS	Fetal Muscle Trunk	muscle
18	chr11:71497200-71497800	Flanking Active TSS	Dnd41	blood
19	chr11:71497200-71497800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr11:71497200-71498400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
21	chr11:71497200-71498600	Active TSS	Skeletal Muscle Female	skeletal muscle
22	chr11:71497200-71498600	Active TSS	Stomach Smooth Muscle	stomach
23	chr11:71497200-71498800	Active TSS	Fetal Muscle Leg	muscle
24	chr11:71497200-71498800	Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr11:71497200-71498800	Active TSS	NH-A	brain
26	chr11:71497200-71499000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr11:71497200-71499000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:71497200-71499000	Active TSS	Primary T killer memory cells from peripheral blood	blood
29	chr11:71497200-71499000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:71497200-71499000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr11:71497200-71499000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr11:71497200-71499000	Active TSS	Duodenum Mucosa	Duodenum
33	chr11:71497200-71499000	Active TSS	Fetal Brain Female	brain
34	chr11:71497200-71499000	Active TSS	NHEK	skin
35	chr11:71497200-71499200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr11:71497200-71499200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr11:71497200-71499200	Active TSS	Brain Anterior Caudate	brain
38	chr11:71497200-71499200	Active TSS	Brain Cingulate Gyrus	brain
39	chr11:71497200-71499200	Active TSS	Fetal Lung	lung
40	chr11:71497200-71499200	Active TSS	Thymus	Thymus
41	chr11:71497200-71499400	Active TSS	H9 Cell Line	embryonic stem cell
42	chr11:71497200-71499400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:71497200-71499400	Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr11:71497200-71499400	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr11:71497200-71499400	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr11:71497200-71499400	Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr11:71497200-71499400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
48	chr11:71497200-71499400	Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr11:71497200-71499400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr11:71497200-71499400	Active TSS	Rectal Smooth Muscle	rectum

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