| Tag | Content |
|---|
EnhancerAtlas ID | HS095-09414 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr14:90979600-90980630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr14:90980048-90980059 | TCCTGTTTACT | + | 6.32 | | Myog | MA0500.1 | chr14:90979780-90979791 | CCGCAGCTGTC | - | 6.32 |
|
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_03967 | chr14:90977506-90981551 | Brain_Anterior_Caudate | | SE_05763 | chr14:90977461-90990749 | Brain_Cingulate_Gyrus | | SE_06526 | chr14:90975827-90992794 | Brain_Hippocampus_Middle | | SE_24186 | chr14:90978224-90980896 | Colon_Crypt_2 | | SE_28244 | chr14:90977561-90981612 | Fetal_Intestine | | SE_29280 | chr14:90977514-90981571 | Fetal_Intestine_Large | | SE_31992 | chr14:90977580-90981435 | Gastric | | SE_33611 | chr14:90974537-90981544 | H2171 | | SE_41893 | chr14:90978205-90981022 | LNCaP | | SE_47878 | chr14:90978319-90980144 | Pancreas | | SE_47878 | chr14:90980189-90980919 | Pancreas | | SE_65518 | chr14:90974579-90981557 | Pancreatic_islets | | SE_66921 | chr14:90974537-90981544 | H2171 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I090511 | chr14 | 90977667 | 90981615 |
|
Enhancer Sequence | ATGACTCAAG TTGTTCTCTG CCTCCAAGGG CCTGGTTCCA GAAAATTCTG GGTGGAGGTG 60
AGCTGGGCAG CCTCCCTCTA ACCTCCCCGG GGAATGGCCT GGGGACTTAG CCAAACGCTG 120
ACAACCAGTG TGTGAGGGAC AGGTGGACGC TTCCCAAATC AGCTCTGTGC AGAGGACAGA 180
CCGCAGCTGT CAGGCCTATG TTGGCCTGAC CCTCCCCTGT GACCTTGGGC CAGGGACCCC 240
CTCCAGTGTC AGCGTCCCCA TCAGAGCCTC AAGAGCTGAG CCAAGTGACC CTTCTGATGC 300
TCCCTAGCCC TGCCACTCAG CTCCAGCTCA GCCCCAGGGA AGCCCCTCCA CTGTGGGGAC 360
TCACCTGGAG CTACCTGGGG CATGAGCAGC TGAGGAAGGA AAGAAAATGC TCTTTAAGTT 420
GTCATAACAG AGCGGGGCCT CCAGCACCTC CTGTTTACTG AAGGTGAGTA AATACAGCCG 480
GGCCCTTAGC AACAGGCACA AAGGGGCCCT TGTGCCGCCC GCTGCTCGCT GCTCGCTGCT 540
CCCTTGGCTC CCTCCCTGAG CTCAGCCCCA GCTGGGAGCT CTCTGAGAGG CAGGCTGGCC 600
TGGCCCACAG CCCTGGCCTG ACTGGGTGGG GAACGGGGCG GGTGCAAGGA CTGCTGTGTG 660
CCAGTCTCCA GGCGTGTCAG GGAGCCAGGC CTTTAGAGGG CCCTGTCCTC TGCAGGCAGA 720
AAATTCCACC CCATTCTTCT GACCAGCAAA CTGGGGTTCT GAGAGGCCCC TGATTTGAGT 780
TTGTCACTCA GAGATGGAGC GGGTGAGCCT TAGACCAAGA AGCCCTGAGT TGGACGTCAG 840
TCTCGGCCAT GGGCGCTTTG GCGTGTTCTG TGTTACGAGT CCCAGTCTCT TCATTTCTAA 900
CAAGGGGCTC ATGCATCACG CCTGGCTCAC CTGGCTGCGT GCGCATCAAA TCAGATGAGT 960
GTGTGAGGAC GTTCATTCTA AACTTTACAA GCTCTGAGCA AACAGAGGGA GTTATTATTG 1020
GGCCAAGCGG 1030
|
