Variant report

Variant	rs680413
Chromosome Location	chr11:65190379-65190380
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:118)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:118 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:65189745..65191975-chr6:26031207..26033394,2	K562	blood:
2	chr11:65188099..65190744-chr14:77494274..77497074,3	MCF-7	breast:
3	chr11:65190020..65190882-chr3:57678330..57679124,3	Hela-S3	cervix:
4	chr11:65190235..65190950-chr19:18391876..18392576,3	Hela-S3	cervix:
5	chr1:153963058..153963718-chr11:65189844..65190716,2	Hela-S3	cervix:
6	chr11:65190054..65190813-chr2:241499557..241500227,2	Hela-S3	cervix:
7	chr11:65188897..65190954-chr4:1242152..1244163,2	MCF-7	breast:
8	chr11:65082107..65083673-chr11:65189217..65191365,2	MCF-7	breast:
9	chr11:65189010..65195293-chr11:65321323..65327708,15	K562	blood:
10	chr11:65190371..65192936-chr6:31618230..31620421,2	MCF-7	breast:
11	chr11:65190238..65193171-chr13:92003562..92006013,2	K562	blood:
12	chr11:65189906..65190629-chr17:73775381..73775970,2	Hela-S3	cervix:
13	chr1:145381546..145383124-chr11:65189414..65191073,2	MCF-7	breast:
14	chr11:65190297..65191106-chr3:13462431..13463285,2	Hela-S3	cervix:
15	chr11:65190254..65190996-chr19:41257060..41258041,2	Hela-S3	cervix:
16	chr10:27530518..27532485-chr11:65188635..65191492,2	MCF-7	breast:
17	chr11:62607615..62610579-chr11:65189094..65191693,2	MCF-7	breast:
18	chr11:65187744..65191441-chr11:65307194..65309813,3	MCF-7	breast:
19	chr11:65189923..65190738-chr12:110561918..110562871,2	Hela-S3	cervix:
20	chr11:65190290..65190990-chr12:52541232..52541860,2	Hela-S3	cervix:
21	chr11:64018454..64020454-chr11:65189395..65191669,2	MCF-7	breast:
22	chr11:65188258..65192947-chr11:65311570..65315780,5	MCF-7	breast:
23	chr10:22604952..22605691-chr11:65190178..65190864,2	Hela-S3	cervix:
24	chr11:65190111..65190616-chr18:29672226..29673180,2	Hela-S3	cervix:
25	chr11:65188857..65190458-chr11:65768140..65769977,2	K562	blood:
26	chr11:65190161..65193929-chr17:59476956..59480011,3	MCF-7	breast:
27	chr11:65028103..65030991-chr11:65188788..65191974,4	K562	blood:
28	chr11:65190169..65191146-chr7:104652934..104653783,2	HCT-116	colon:
29	chr11:65189915..65190490-chr12:49525074..49525854,2	Hela-S3	cervix:
30	chr10:71992867..71993429-chr11:65189991..65190810,2	Hela-S3	cervix:
31	chr11:65190105..65190725-chr17:73662831..73663392,2	Hela-S3	cervix:
32	chr1:52831422..52832054-chr11:65189870..65190568,2	Hela-S3	cervix:
33	chr1:179846797..179847361-chr11:65190227..65191159,2	Hela-S3	cervix:
34	chr11:65188740..65190659-chr17:59487538..59489067,2	MCF-7	breast:
35	chr11:65189864..65190582-chr5:217801..218515,2	Hela-S3	cervix:
36	chr11:65190115..65190731-chr5:14664107..14664931,2	Hela-S3	cervix:
37	chr11:65190376..65191175-chr11:65267004..65267858,2	Hela-S3	cervix:
38	chr11:65190155..65191154-chr5:108083330..108084319,2	Hela-S3	cervix:
39	chr11:64900564..64902605-chr11:65189487..65191072,2	MCF-7	breast:
40	chr11:65027099..65029284-chr11:65187685..65190495,2	MCF-7	breast:
41	chr1:150551832..150552410-chr11:65190162..65190975,3	Hela-S3	cervix:
42	chr11:65186294..65191468-chr11:65379126..65384544,8	MCF-7	breast:
43	chr11:65190162..65194738-chr11:65316952..65321274,6	K562	blood:
44	chr10:101380169..101381156-chr11:65190137..65191035,3	Hela-S3	cervix:
45	chr11:65178877..65218546-chr11:65218612..65286191,1014	K562	blood:
46	chr11:65183635..65190622-chr11:65305653..65310980,8	MCF-7	breast:
47	chr11:65184392..65191686-chr11:65339528..65345365,10	K562	blood:
48	chr11:65188862..65190415-chr3:63844051..63846487,2	MCF-7	breast:
49	chr11:65190225..65190828-chr12:52449138..52450079,2	Hela-S3	cervix:
50	chr10:3826923..3827869-chr11:65190313..65191133,2	Hela-S3	cervix:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LTBP3-2	chr11:65189793-65190665	NONHSAT022110

No data

Variant related genes	Relation type
ENSG00000077147	Chromatin interaction
ENSG00000100664	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000266173	Chromatin interaction
ENSG00000145390	Chromatin interaction
ENSG00000246090	Chromatin interaction
ENSG00000151422	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000014138	Chromatin interaction
ENSG00000104064	Chromatin interaction
ENSG00000173442	Chromatin interaction
ENSG00000219545	Chromatin interaction
ENSG00000197451	Chromatin interaction
ENSG00000147164	Chromatin interaction
ENSG00000124181	Chromatin interaction
ENSG00000167553	Chromatin interaction
ENSG00000140443	Chromatin interaction
ENSG00000206652	Chromatin interaction
ENSG00000140474	Chromatin interaction
ENSG00000188542	Chromatin interaction
ENSG00000175334	Chromatin interaction
ENSG00000014216	Chromatin interaction
ENSG00000179262	Chromatin interaction
ENSG00000154124	Chromatin interaction
ENSG00000176973	Chromatin interaction
ENSG00000173465	Chromatin interaction
ENSG00000148344	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000159692	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000215417	Chromatin interaction
ENSG00000197818	Chromatin interaction
ENSG00000070444	Chromatin interaction
ENSG00000228393	Chromatin interaction
ENSG00000142186	Chromatin interaction
ENSG00000106211	Chromatin interaction
ENSG00000122970	Chromatin interaction
ENSG00000078124	Chromatin interaction
ENSG00000178636	Chromatin interaction
ENSG00000198805	Chromatin interaction
ENSG00000073578	Chromatin interaction
ENSG00000164366	Chromatin interaction
ENSG00000054118	Chromatin interaction
ENSG00000199038	Chromatin interaction
ENSG00000107897	Chromatin interaction
ENSG00000174516	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000162298	Chromatin interaction
ENSG00000161526	Chromatin interaction
ENSG00000233396	Chromatin interaction
ENSG00000129480	Chromatin interaction
ENSG00000174839	Chromatin interaction
ENSG00000175376	Chromatin interaction
ENSG00000180817	Chromatin interaction
ENSG00000154222	Chromatin interaction
ENSG00000169905	Chromatin interaction
ENSG00000155256	Chromatin interaction
ENSG00000162241	Chromatin interaction
ENSG00000177125	Chromatin interaction
ENSG00000186854	Chromatin interaction
ENSG00000149782	Chromatin interaction
ENSG00000123358	Chromatin interaction
ENSG00000134758	Chromatin interaction
ENSG00000260475	Chromatin interaction
ENSG00000107438	Chromatin interaction
ENSG00000141385	Chromatin interaction
ENSG00000129250	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000203875	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000155287	Chromatin interaction
ENSG00000188493	Chromatin interaction
ENSG00000177954	Chromatin interaction
ENSG00000086189	Chromatin interaction
ENSG00000230513	Chromatin interaction
ENSG00000077312	Chromatin interaction
ENSG00000268366	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000196388	Chromatin interaction
ENSG00000247095	Chromatin interaction
ENSG00000102580	Chromatin interaction
ENSG00000260233	Chromatin interaction
ENSG00000240549	Chromatin interaction
ENSG00000241933	Chromatin interaction
ENSG00000179218	Chromatin interaction
ENSG00000258017	Chromatin interaction
ENSG00000261360	Chromatin interaction
ENSG00000269897	Chromatin interaction
ENSG00000172757	Chromatin interaction
ENSG00000270526	Chromatin interaction
ENSG00000196810	Chromatin interaction
ENSG00000067082	Chromatin interaction
ENSG00000263800	Chromatin interaction
ENSG00000262412	Chromatin interaction
ENSG00000086200	Chromatin interaction
ENSG00000273003	Chromatin interaction
ENSG00000108469	Chromatin interaction
ENSG00000148444	Chromatin interaction
ENSG00000247400	Chromatin interaction
ENSG00000106399	Chromatin interaction
ENSG00000175315	Chromatin interaction
ENSG00000172732	Chromatin interaction
ENSG00000119669	Chromatin interaction
ENSG00000159346	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000197894	Chromatin interaction
ENSG00000201558	Chromatin interaction
ENSG00000168056	Chromatin interaction
ENSG00000258101	Chromatin interaction
ENSG00000173727	Chromatin interaction
ENSG00000123416	Chromatin interaction
ENSG00000255992	Chromatin interaction
ENSG00000196866	Chromatin interaction
ENSG00000184436	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000143384	Chromatin interaction
ENSG00000149798	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000256018	Chromatin interaction
ENSG00000144504	Chromatin interaction
ENSG00000171940	Chromatin interaction
ENSG00000213465	Chromatin interaction
ENSG00000122958	Chromatin interaction
ENSG00000244879	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000203546	Chromatin interaction
ENSG00000175592	Chromatin interaction
ENSG00000177192	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11602839	1.00[CHB][hapmap]
rs1205739	1.00[EUR][1000 genomes]
rs2073801	1.00[CHB][hapmap]
rs2239895	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2904976	1.00[CHB][hapmap];0.80[CHD][hapmap]
rs3741384	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs573864	0.90[CHB][hapmap];0.83[JPT][hapmap];1.00[EUR][1000 genomes]
rs666834	1.00[CHB][hapmap];0.80[CHD][hapmap];0.80[ASN][1000 genomes]
rs7925823	0.91[CHB][hapmap];0.87[CHD][hapmap];0.93[GIH][hapmap];0.83[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526181	chr11:64638041-65257329	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic 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	1539 gene(s)	inside rSNPs	diseases
2	esv2422285	chr11:65013294-65254540	Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong 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	474 gene(s)	inside rSNPs	diseases
3	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
4	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
5	nsv541065	chr11:65117387-65271894	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	835 gene(s)	inside rSNPs	diseases
6	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
7	nsv897717	chr11:65140209-65278461	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic 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	942 gene(s)	inside rSNPs	diseases
8	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
9	nsv541066	chr11:65142779-65271894	Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers 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	833 gene(s)	inside rSNPs	diseases
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65183600-65194200	Flanking Active TSS	Primary B cells from cord blood	blood
2	chr11:65186000-65193800	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr11:65186000-65195000	Transcr. at gene 5' and 3'	Duodenum Smooth Muscle	Duodenum
4	chr11:65186200-65192400	Active TSS	Right Ventricle	heart
5	chr11:65186200-65197400	Active TSS	Psoas Muscle	Psoas
6	chr11:65186800-65191800	Flanking Active TSS	Primary hematopoietic stem cells	blood
7	chr11:65188000-65194200	Active TSS	Liver	Liver
8	chr11:65188400-65191400	Active TSS	Left Ventricle	heart
9	chr11:65188400-65191800	Active TSS	Sigmoid Colon	Sigmoid Colon
10	chr11:65188400-65193600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr11:65188400-65194400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
12	chr11:65188400-65194600	Active TSS	Esophagus	oesophagus
13	chr11:65188600-65190400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:65188600-65190400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:65188600-65190400	Active TSS	Fetal Brain Female	brain
16	chr11:65188600-65190400	Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr11:65188600-65190800	Active TSS	Breast Myoepithelial Primary Cells	Breast
18	chr11:65188600-65190800	Active TSS	Primary T helper naive cells from peripheral blood	blood
19	chr11:65188600-65190800	Active TSS	Colon Smooth Muscle	Colon
20	chr11:65188600-65190800	Active TSS	Stomach Mucosa	stomach
21	chr11:65188600-65190800	Active TSS	A549	lung
22	chr11:65188600-65190800	Active TSS	Monocytes-CD14+_RO01746	blood
23	chr11:65188600-65191000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:65188600-65191400	Active TSS	Aorta	Aorta
25	chr11:65188600-65191600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr11:65188600-65193000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr11:65188600-65194000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
28	chr11:65188600-65194000	Active TSS	HSMMtube	muscle
29	chr11:65188800-65190600	Active TSS	H9 Cell Line	embryonic stem cell
30	chr11:65188800-65194000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
31	chr11:65188800-65194000	Active TSS	Lung	lung
32	chr11:65189000-65193600	Active TSS	Spleen	Spleen
33	chr11:65189000-65193800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chr11:65189000-65194600	Active TSS	Pancreas	Pancrea
35	chr11:65189200-65190400	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr11:65189200-65190400	Active TSS	Primary T cells from cord blood	blood
37	chr11:65189200-65190400	Active TSS	Rectal Smooth Muscle	rectum
38	chr11:65189200-65190400	Active TSS	K562	blood
39	chr11:65189200-65191000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr11:65189200-65191200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
41	chr11:65189200-65191400	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr11:65189200-65191400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:65189200-65191400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr11:65189200-65191400	Active TSS	Brain Anterior Caudate	brain
45	chr11:65189200-65191400	Active TSS	Brain Cingulate Gyrus	brain
46	chr11:65189200-65191600	Active TSS	Brain Substantia Nigra	brain
47	chr11:65189200-65191800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr11:65189200-65191800	Active TSS	HSMM	muscle
49	chr11:65189200-65192800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr11:65189200-65193000	Bivalent/Poised TSS	HepG2	liver

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