| Tag | Content |
|---|
EnhancerAtlas ID | HS047-13773 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:2898760-2900010 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr17:2899831-2899844 | GAATGTTCCAGAA | - | 6.67 | | MSC | MA0665.1 | chr17:2899346-2899356 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr17:2899346-2899356 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr17:2899346-2899356 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr17:2899346-2899356 | AACAGCTGTT | - | 6.02 | | Zfx | MA0146.2 | chr17:2899944-2899958 | CCGGCCTGGGCCTG | + | 6.71 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_31401 | chr17:2898311-2901047 | Gastric | | SE_41971 | chr17:2898312-2900026 | LNCaP | | SE_65245 | chr17:2897393-2900761 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I002995 | chr17 | 2898455 | 2900850 |
|
Enhancer Sequence | GTAACCTGGT TTGGGAGGGC TTTGGGAGCC CAGGGCGGGC GAGGTGAGGG CCTGCCTCTG 60
GTCTGACCTG CTAAGAGGCT GTGGCCGTCC CCATATTCGT TCCCGTAGCC GGCCATTCGT 120
TCAGCTGCGC AGCAGCGTCA CAGTCCGTTC TGCTGTGTTT CTGGCCGAGG CTGTGCCTCA 180
GCGGTCCGTT CTGTTGTGTT TCTGGCCGAG GCCACACCTC AGGGGCCCTG GGCGGGAGGC 240
GGGGCAGAGC TTGTGTTTCT TCCACGTTGA CTGATGGGAA AACTGCAGCC CATGGTGGTG 300
ACAAGACTTC CTTGAGGTTT CTCCGTTTAT CAGGGGCAGA GCCCAGGGCA GAGCCTGGGG 360
GCCCTGGTCA TAGAGGGTGG TGGCAAAGGG TGCATGGTGG GGTTTGCAGA TGGGGGCCTG 420
AAGCCGCCTG TGCCACTTTG GAGCGTGTGA CTCTGGGCAA GCCAGTTAAC CTTCTCATCT 480
ATAAAATGGG GGGTAACACC ACCCATGGTA GAGGGTGATT GTGGGGATTA CATACATTTC 540
TGACTAGGGT TCATACGATG CCCAATTCAT GGCTGGCTTC CTATAGAACA GCTGTTCACT 600
GTCCAGCCCC TGGTCATTTT GTCCCCCTTC CTGCCCCAGT GACGGAAGGC TGGTTATTGC 660
GTGAGAATCC TTCCCCACCC CCAGCCTTCC TCATCTCACA GGCTCCTCTC TCACCACACC 720
TGTGGGAATT CAGCCTTGAC CTCCACTAGG GAGACCTGGA CGAGACCCCT GTCCCCACTG 780
CTTTCCTGCC GTGCCCCCCG TTTGCTGCTC TGACAGCCGT GCATCCCTGG GGAGAGCCGC 840
GGCTGGTTCC TGGCTGTTAC AAGCCCAGTT CCCCCAGCCT GCCTTCTGCC CCTTTTCAGT 900
CTGGGAAAAT AAGAAAATGC AGGCAGGCCT TTGCCCAAAC TCTGACCTGT GTGTCTCTGA 960
GCAGGAACTG GGGAGGGAGC ACAGATGTAA AATTGTAAAC ATAGTGCCTG GCTTCTTAGG 1020
AAAGAAGGAA ATTGGCAAAC GAGATGATGA GTTGGCTCTA AAATAGCTAC TGAATGTTCC 1080
AGAAACAAAT GGAAGCAGAA ATCCTTTTGT ATCCAAAGTG GGTTTTCATT CAACCTTTCA 1140
CCTCCAGCCC CTCTGTTCCC TTATGGCCTC TCTCACCTGC TGCCCCGGCC TGGGCCTGAG 1200
GCCTGTTCTC TCTGGGCCTT CTCAGTCTTA TGTGTGTTTC TTGGGAAATA 1250
|
