| Tag | Content |
|---|
EnhancerAtlas ID | HS037-34786 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr6:158374950-158376300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr6:158375713-158375729 | CCTGGACTTTAACCCC | - | 6.7 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23621 | chr6:158372548-158376467 | Colon_Crypt_1 | | SE_24200 | chr6:158373708-158376361 | Colon_Crypt_2 | | SE_28168 | chr6:158372423-158377079 | Fetal_Intestine | | SE_29030 | chr6:158372269-158377129 | Fetal_Intestine_Large | | SE_65268 | chr6:158373454-158376617 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I157951 | chr6 | 158372557 | 158376989 |
|
Enhancer Sequence | AGGGTCTGGT GAGTGGGATC ACGTCAGCAG AGCTCATTTC CTGCATGTGA TTCTACTACT 60
ACCTTCTACT ACTACCCTCC CTTTACCGCT GCACTCAGTC ATTATTTCTA TCTGATAGCT 120
TAAAAAAAAC AAAATAGAAA ACCACTACTC ATACCTGACC CCCCAAAATA TACTGGTAGC 180
TGCTCAGAGG ACAGAATTAA TTTTAAAAAT AATCTAAATT AGGCAAACAG AGCGTGAGAA 240
GCCGATAATC ACGCAACTCC CTCCAGAAAA GGAAGTGGAG CAGGCGGGCG CCCAGCTGCA 300
AGCCCTCAGA AGGCTCAGCC TCCAGCGCCA GGACCTGATT TTATTACTAA CAAGGTGCGG 360
TCCTCATTCT TTGGGTCTGC CACATGCCTC ACGGTAATTT TCCAGGCAAA CTATATCACA 420
TGATACTGGC TTTACTGTCC AAGCAATAAG CGCAGAGTCT CTGGCAGTTT GGACTTCTCT 480
GAGATTGCAC TGCTGAGCAC GTAGCTGCGG CGGTCACAGG AACTCACATG CCAAAGAACT 540
GGGAAGAATG TTTTAAAAAC CTGGAAAGAA CCGGTTTCCT TTTCTGCAGC CTAACAAATA 600
CCTCCTTGAG GGAAGTAGGA AGCTTTCAGA ACTCCCTCAC TATCCAGAGG CTTATCATTG 660
TGTGAAGGAT CAGAGTTTGT CAAGGCAAAG AGAATCAAAA CTATTTACTC AGGCTTGGAA 720
TTGATCAGGT GCTCGGGAGG CTCGGAGCAG GGGAGCGGCG GCTCCTGGAC TTTAACCCCC 780
GTGTTTGTGG AAGCAGTGAC TATGATGATG ATAGGAGAGC TGGCGCCCTC ACGCGCTTGT 840
CACCTGCTGC GGGCATCAGT GAGCGCTTGC TGCCGCCTCT GAGATAAGGA GGGCTCTGTA 900
GAAACTCACC TGGGCCACCT CCACTCGGAA GCCCTCCTTT CTTTCCTGCT AGACAAGAAG 960
CGCCTGGAGC AGCCGAGGGA ACACACCTGG TGGCAACGCC TGGTTCCCAC TTTCGAACCT 1020
CAGGATTGAG AGAGGGATGA ACGCGGGAAG TCTGAGGACA CACTCTGTCC TGCCCTTAAC 1080
TGTGACTGTC CGAGCCACCT AGGGGGACAC GTGGGAGGCA GTCCCAGGGA GGCTGTACTA 1140
GAGAGGTGCT GCCCCCAACA GAAGCCGGGA GTCCCTGCCT GGGCCCAAGC TCCTGCCATT 1200
CTCTAAGTGA TGCAGAGAGG GCCCCACCGC CGGGAGGGGC TTTCTGGCAC AGCTGTTCTC 1260
GCCCCTGCAC TCTGAAGAAG AGTAGATACC TAGATACAGT AAGTAAAGGA AAAGAACTGA 1320
GCATTTCTCT CCCTTTTTAG GAGGACCATC 1350
|
