Variant report

Variant	rs71462347
Chromosome Location	chr11:65308164-65308165
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	MYC	chr11:65307631-65308700	K562	blood:	n/a	chr11:65308306-65308316
2	STAT3	chr11:65308136-65308565	MCF10A-Er-Src	breast:	n/a	chr11:65308314-65308326 chr11:65308447-65308459
3	POLR2A	chr11:65307717-65308536	Raji	blood:	n/a	n/a
4	FOXA1	chr11:65307909-65308679	T-47D	breast:	n/a	n/a
5	MAX	chr11:65307648-65308696	SK-N-SH	brain:	n/a	chr11:65308306-65308316
6	MYC	chr11:65307125-65308532	MCF-7	breast:	n/a	chr11:65307431-65307440 chr11:65307430-65307441 chr11:65307429-65307442 chr11:65307431-65307440 chr11:65308306-65308316
7	MAX	chr11:65306379-65308620	H1-hESC	embryonic stem cell:	n/a	chr11:65307431-65307440 chr11:65307430-65307441 chr11:65307429-65307442 chr11:65307431-65307440 chr11:65308306-65308316
8	POLR2A	chr11:65307616-65308716	K562	blood:	n/a	n/a
9	POLR2A	chr11:65307918-65308674	SK-N-MC	brain:	n/a	n/a
10	TRIM28	chr11:65308116-65308774	K562	blood:	n/a	n/a
11	CHD2	chr11:65307739-65308718	GM12878	blood:	n/a	chr11:65308309-65308319
12	YY1	chr11:65307937-65308314	HCT-116	colon:	n/a	n/a
13	BCL3	chr11:65307636-65308628	A549	lung:	n/a	chr11:65308316-65308329 chr11:65308271-65308284 chr11:65307943-65307952
14	TCF12	chr11:65307021-65308864	ECC-1	luminal epithelium:	n/a	chr11:65308225-65308232 chr11:65307362-65307369
15	TFAP2A	chr11:65307737-65308577	Hela-S3	cervix:	n/a	chr11:65307937-65307948 chr11:65308169-65308184 chr11:65307937-65307949 chr11:65308128-65308139 chr11:65308489-65308504
16	POLR2A	chr11:65307414-65308180	Hela-S3	cervix:	n/a	n/a
17	MTA3	chr11:65307674-65308172	GM12878	blood:	n/a	n/a
18	MAZ	chr11:65307341-65308728	Hela-S3	cervix:	n/a	chr11:65307431-65307440 chr11:65307430-65307441 chr11:65307429-65307442 chr11:65307431-65307440 chr11:65308306-65308316
19	RAD21	chr11:65307217-65308878	ECC-1	luminal epithelium:	n/a	n/a
20	POLR2A	chr11:65307670-65308660	SK-N-SH	brain:	n/a	n/a
21	NR2F2	chr11:65307071-65308821	MCF-7	breast:	n/a	n/a
22	SP1	chr11:65307611-65308768	A549	lung:	n/a	chr11:65307938-65307952 chr11:65307942-65307951 chr11:65308452-65308466 chr11:65307672-65307682 chr11:65308204-65308216 chr11:65307672-65307686 chr11:65307673-65307682 chr11:65308192-65308201 chr11:65308133-65308143 chr11:65308206-65308215 chr11:65307943-65307952 chr11:65308228-65308240 chr11:65307941-65307953 chr11:65308172-65308184 chr11:65307672-65307681 chr11:65307672-65307681 chr11:65308316-65308328 chr11:65307671-65307683 chr11:65307671-65307683 chr11:65308191-65308201 chr11:65307941-65307953 chr11:65308190-65308202 chr11:65308191-65308201 chr11:65308174-65308183 chr11:65308204-65308216 chr11:65308190-65308202 chr11:65308191-65308200 chr11:65308192-65308201 chr11:65307672-65307682 chr11:65308230-65308239
23	CTCF	chr11:65307559-65308790	K562	blood:	n/a	chr11:65307933-65307951 chr11:65307936-65307949 chr11:65307936-65307949
24	JUND	chr11:65308117-65308754	A549	lung:	n/a	chr11:65308312-65308321
25	E2F4	chr11:65307729-65308601	MCF10A-Er-Src	breast:	n/a	chr11:65308209-65308219 chr11:65308229-65308238 chr11:65308495-65308504
26	EGR1	chr11:65307224-65308359	ECC-1	luminal epithelium:	n/a	chr11:65307636-65307651 chr11:65308134-65308147 chr11:65307633-65307646 chr11:65307867-65307881 chr11:65307400-65307413
27	EP300	chr11:65306950-65308832	ECC-1	luminal epithelium:	n/a	chr11:65308123-65308139 chr11:65308243-65308259 chr11:65307935-65307951
28	POLR2A	chr11:65301704-65308571	GM12878	blood:	n/a	n/a
29	CREB1	chr11:65307109-65308664	H1-hESC	embryonic stem cell:	n/a	n/a
30	EGR1	chr11:65306545-65308763	HCT-116	colon:	n/a	chr11:65307636-65307651 chr11:65308473-65308486 chr11:65308134-65308147 chr11:65307633-65307646 chr11:65307867-65307881 chr11:65307400-65307413
31	HEY1	chr11:65308160-65308424	K562	blood:	n/a	chr11:65308312-65308327
32	YY1	chr11:65308113-65308697	GM12878	blood:	n/a	chr11:65308314-65308328 chr11:65308495-65308504 chr11:65308431-65308442
33	PAX5	chr11:65307537-65308589	GM12892	blood:	n/a	chr11:65308468-65308477
34	PML	chr11:65307462-65308804	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:65307810-65308485	GM12878	blood:	n/a	n/a
36	ELF1	chr11:65308044-65308656	K562	blood:	n/a	chr11:65308130-65308139
37	SIN3A	chr11:65306531-65308671	H1-hESC	embryonic stem cell:	n/a	chr11:65308326-65308337 chr11:65308253-65308266 chr11:65308431-65308442 chr11:65307430-65307439
38	MAX	chr11:65307155-65308706	MCF-7	breast:	n/a	chr11:65307431-65307440 chr11:65307430-65307441 chr11:65307429-65307442 chr11:65307431-65307440 chr11:65308306-65308316
39	MAX	chr11:65306329-65308735	H1-hESC	embryonic stem cell:	n/a	chr11:65307431-65307440 chr11:65307430-65307441 chr11:65307429-65307442 chr11:65307431-65307440 chr11:65308306-65308316
40	POLR2A	chr11:65307451-65308491	GM15510	blood:	n/a	n/a
41	MAX	chr11:65307355-65308647	GM12878	blood:	n/a	chr11:65307431-65307440 chr11:65307430-65307441 chr11:65307429-65307442 chr11:65307431-65307440 chr11:65308306-65308316
42	POLR2A	chr11:65307035-65308872	MCF-7	breast:	n/a	n/a
43	POLR2A	chr11:65307775-65308956	U87	brain:	n/a	n/a
44	HCFC1	chr11:65307674-65308665	K562	blood:	n/a	n/a
45	MYC	chr11:65307531-65308610	MCF10A-Er-Src	breast:	n/a	chr11:65308306-65308316
46	SMC3	chr11:65307568-65308745	Hela-S3	cervix:	n/a	chr11:65307935-65307949
47	E2F4	chr11:65307922-65308491	K562	blood:	n/a	chr11:65308209-65308219 chr11:65308229-65308238
48	PBX3	chr11:65307702-65308680	A549	lung:	n/a	n/a
49	FOXM1	chr11:65307654-65308669	GM12878	blood:	n/a	n/a
50	TCF7L2	chr11:65307762-65308531	HCT-116	colon:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65306570..65308318-chr11:65381821..65384190,3	K562	blood:
2	chr11:65307403..65309183-chr11:65336934..65338289,13	MCF-7	breast:
3	chr11:65307335..65308296-chr17:73775501..73776065,2	HCT-116	colon:
4	chr11:65307252..65310035-chr11:65625535..65628177,3	K562	blood:
5	chr11:65100032..65102632-chr11:65307572..65309259,3	MCF-7	breast:
6	chr11:65307733..65308892-chr11:65339050..65340029,8	K562	blood:
7	chr11:65187744..65191441-chr11:65307194..65309813,3	MCF-7	breast:
8	chr11:65306479..65309303-chr5:10247983..10249958,2	MCF-7	breast:
9	chr11:65307679..65310014-chr11:65429997..65432824,2	MCF-7	breast:
10	chr1:29063672..29064279-chr11:65307848..65308494,2	HCT-116	colon:
11	chr11:65263261..65267812-chr11:65306192..65309215,4	MCF-7	breast:
12	chr11:65308066..65308605-chr11:65337068..65337929,2	Hela-S3	cervix:
13	chr11:65183635..65190622-chr11:65305653..65310980,8	MCF-7	breast:
14	chr11:65307860..65308586-chr11:65319285..65320130,2	K562	blood:
15	chr11:65307697..65309026-chr3:64008900..64009738,3	MCF-7	breast:
16	chr11:65307609..65308998-chr11:65336892..65338725,9	K562	blood:
17	chr11:65266245..65270118-chr11:65305867..65309860,5	MCF-7	breast:
18	chr11:65307312..65308926-chr11:65339023..65340083,15	MCF-7	breast:
19	chr11:65189854..65192035-chr11:65305464..65309123,3	K562	blood:
20	chr11:65307648..65308488-chr11:65318954..65319482,2	MCF-7	breast:
21	chr11:65307871..65308546-chr11:65343015..65343628,2	K562	blood:
22	chr11:65306623..65309907-chr11:65380382..65384254,6	MCF-7	breast:

Variant related genes	Relation type
LTBP3	TF binding region
ENSG00000251562	Chromatin interaction
ENSG00000172757	Chromatin interaction
ENSG00000173039	Chromatin interaction
ENSG00000248968	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000133884	Chromatin interaction
ENSG00000176973	Chromatin interaction
ENSG00000173442	Chromatin interaction
ENSG00000163636	Chromatin interaction
ENSG00000198492	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000173465	Chromatin interaction
ENSG00000172732	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000168056	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000260233	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11545200	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11600543	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11602375	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11604369	0.92[EUR][1000 genomes]
rs11605810	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11605937	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1194337	0.90[EUR][1000 genomes]
rs12799784	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34789990	0.88[EUR][1000 genomes]
rs35111506	0.84[EUR][1000 genomes]
rs35138901	0.92[EUR][1000 genomes]
rs36085849	0.84[EUR][1000 genomes]
rs3782089	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7935877	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897715	chr11:65083491-65427346	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
2	nsv897716	chr11:65083491-65481166	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS 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	999 gene(s)	inside rSNPs	diseases
3	esv1829999	chr11:65136686-65343124	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	963 gene(s)	inside rSNPs	diseases
4	nsv897718	chr11:65140209-65577516	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1003 gene(s)	inside rSNPs	diseases
5	nsv541067	chr11:65142779-65313799	Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	950 gene(s)	inside rSNPs	diseases
6	nsv541068	chr11:65142779-65331136	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	953 gene(s)	inside rSNPs	diseases
7	nsv541069	chr11:65142779-65368787	Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	965 gene(s)	inside rSNPs	diseases
8	nsv541070	chr11:65142779-65397058	Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription 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 miRNA target site	972 gene(s)	inside rSNPs	diseases
9	nsv541071	chr11:65142779-65429352	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
10	nsv897719	chr11:65157094-65335705	Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
11	nsv541072	chr11:65171202-65313799	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	946 gene(s)	inside rSNPs	diseases
12	nsv541073	chr11:65171202-65331136	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
13	nsv541074	chr11:65171202-65368787	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	961 gene(s)	inside rSNPs	diseases
14	nsv541075	chr11:65210592-65331136	Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	620 gene(s)	inside rSNPs	diseases
15	nsv541076	chr11:65210592-65397058	Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	645 gene(s)	inside rSNPs	diseases
16	nsv897720	chr11:65213434-65445950	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' 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	665 gene(s)	inside rSNPs	diseases
17	nsv897721	chr11:65278461-65422853	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
18	nsv897722	chr11:65278461-65436888	Genic enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
19	nsv897723	chr11:65294830-65481166	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers 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	107 gene(s)	inside rSNPs	diseases
20	nsv897724	chr11:65300252-65309514	Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
21	nsv897725	chr11:65300252-65311405	Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases
22	nsv897726	chr11:65300252-65318871	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	28 gene(s)	inside rSNPs	diseases
23	nsv897727	chr11:65302893-65311405	Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases
24	nsv897728	chr11:65302893-65318871	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	28 gene(s)	inside rSNPs	diseases
25	nsv897729	chr11:65302893-65322548	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	30 gene(s)	inside rSNPs	diseases
26	nsv897730	chr11:65302893-65376484	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
27	esv3413523	chr11:65302976-65308274	Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
28	nsv897731	chr11:65304592-65318871	Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65297400-65311200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:65302000-65309600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:65304600-65311800	Weak transcription	HepG2	liver
4	chr11:65305200-65309200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:65306200-65308600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
6	chr11:65306200-65308600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
7	chr11:65306200-65308600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
8	chr11:65306200-65308800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
9	chr11:65306400-65308200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
10	chr11:65306400-65308400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:65306400-65308600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
12	chr11:65306400-65308600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
13	chr11:65306400-65308800	Active TSS	H9 Cell Line	embryonic stem cell
14	chr11:65306400-65308800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
15	chr11:65306600-65308600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr11:65307000-65308200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr11:65307000-65308800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr11:65307000-65309600	Flanking Active TSS	HMEC	breast
19	chr11:65307200-65308200	Flanking Active TSS	Adipose Nuclei	Adipose
20	chr11:65307200-65308200	Flanking Active TSS	Right Ventricle	heart
21	chr11:65307200-65308400	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr11:65307200-65308400	Active TSS	Primary B cells from peripheral blood	blood
23	chr11:65307200-65308400	Active TSS	Fetal Intestine Small	intestine
24	chr11:65307200-65308600	Active TSS	Primary T cells from cord blood	blood
25	chr11:65307200-65308600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
26	chr11:65307200-65308600	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr11:65307200-65308600	Active TSS	Colon Smooth Muscle	Colon
28	chr11:65307200-65308600	Active TSS	Duodenum Mucosa	Duodenum
29	chr11:65307200-65308600	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr11:65307200-65308800	Flanking Active TSS	Primary B cells from cord blood	blood
31	chr11:65307200-65308800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr11:65307200-65309000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr11:65307200-65309000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
34	chr11:65307200-65309000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr11:65307200-65309000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
36	chr11:65307200-65309200	Flanking Active TSS	Colonic Mucosa	Colon
37	chr11:65307200-65309400	Flanking Active TSS	Stomach Smooth Muscle	stomach
38	chr11:65307200-65322600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:65307400-65308400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr11:65307400-65308400	Active TSS	Esophagus	oesophagus
41	chr11:65307400-65308400	Active TSS	Placenta Amnion	Placenta Amnion
42	chr11:65307400-65308400	Active TSS	Sigmoid Colon	Sigmoid Colon
43	chr11:65307400-65308600	Active TSS	Gastric	stomach
44	chr11:65307400-65308600	Active TSS	Rectal Smooth Muscle	rectum
45	chr11:65307400-65308600	Active TSS	Stomach Mucosa	stomach
46	chr11:65307400-65308600	Active TSS	Thymus	Thymus
47	chr11:65307400-65308600	Active TSS	Hela-S3	cervix
48	chr11:65307400-65308600	Active TSS	NHDF-Ad	bronchial
49	chr11:65307400-65308800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr11:65307400-65308800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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