| Tag | Content |
|---|
EnhancerAtlas ID | HS052-38955 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr9:101760630-101761810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr9:101761318-101761337 | CGGCACCCCCTGGTGGTCA | - | 7.42 | | ESR2 | MA0258.2 | chr9:101761510-101761525 | GGGACAGGCTGACCT | - | 6.85 | | SREBF2 | MA0596.1 | chr9:101761614-101761624 | ATGGGGTGAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_00227 | chr9:101754644-101762414 | Adipose_Nuclei | | SE_26003 | chr9:101758902-101761748 | Duodenum_Smooth_Muscle | | SE_37448 | chr9:101759216-101761861 | HSMMtube | | SE_41309 | chr9:101760473-101762144 | Left_Ventricle | | SE_49203 | chr9:101760474-101761957 | Right_Atrium | | SE_54766 | chr9:101756399-101762040 | Stomach_Smooth_Muscle | | SE_55714 | chr9:101754821-101762101 | u87 | | SE_67541 | chr9:101754821-101762101 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I098997 | chr9 | 101759839 | 101761681 |
|
Enhancer Sequence | GTCTGTGGGT CAGAGAAAGT ATAGAGAACT GGAGAGAAAA AATTGTAGGA TAATTTAATA 60
ACGTCATGAC AGAGCCAAGG AGGCAGGGTG TTGCTGTGGA AATACTGCCC GCTGGGGAGA 120
GTCAGACAGC TTGGAAGGAG GCCCTGCCTA GCCCCCTATT TGCTGTCGGC CTGGGGCAAG 180
TTGCTGATCA GTTTCCAAGC TTCAGATTCC TTAGCCGTCC TCTGGGAGCA TGAACAATCC 240
CCGATGCTGG GTGGATGAGA GGGCTGAATC TGGCCGCAGT TGTGGAAGTG GCTTCTGAAT 300
TGCGAATGCT TTTCTCAGGG GTGGAATTAG GATCTCTCAG CAAGGGGTTA AGGTGAAGGG 360
GCTGGGGCGA GGGCTTTCCT AGACTGAGAA GATGAGGTCC ACGTGGGGAC TGGGCTCTGA 420
TCCCAACGCA GCTCGCCTGT TCCCGGGATC AGCCACACTC CTTATCTAGC AGACAAAAGG 480
TCAGTTGAAA GCAATGGAGC TAGCCAAAGT GTCCTTTTCT TCTTGATGTG TAGACAGCCC 540
GGATGGTGGG AGAAAGCCCT GGCTAAGCAA AGCCCCTAAT ATTTGCATTC AGAGCTTCCC 600
TGACACCATC GTGACCCGTG GAAGGGGCCA CCCCACCTCC TTCTTCCCAG GGGTCAGTCC 660
TTGGAGGACA GGCAATCGGC TGCTTGCACG GCACCCCCTG GTGGTCAGAG CAGGGAAGAC 720
GAGAGTGCTC GACCCGTGCT GGCCACTCTT CCATCACAGG ATGGGACAGG AGTGGGTGGG 780
GAGGGGGGCA GAGTCCTTTG GAGGATTTGG CACCTCTTCC AGAGTTATTG TGACCATGGG 840
ACCTGCGTGA GCACAGCGTG TGTGGGAAGG GCCTGGCCCG GGGACAGGCT GACCTGGCTT 900
CAGGGCCCTT CCCAGTCTCA GTCTCATTCC CAGGGTTAAT AATACTGAGG TATTGATGTG 960
TGGATCCGGC AGGTCACACC TGTCATGGGG TGATAGTGGG ATCCCCAACC AGGATCTGCC 1020
CACCTGCAGG AAGGTGGTGG GAGGGGTCCC GGTGGGCAGG ACAGGTGGGC CAGCAGGAGG 1080
GTTGCTGGAG GGAGTGCATG GGACAATCTT GGCATGGGCC CAGCCATAAC AGGCGTGCAG 1140
TCATGGTAGT ACAACTTCTT TTTCTTCTTC TTCTTCTTCT 1180
|
