| Tag | Content |
|---|
EnhancerAtlas ID | HS052-01048 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:40281740-40282760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr1:40282308-40282320 | TGTGACGTCATC | + | 6.02 | | CREB1 | MA0018.3 | chr1:40282308-40282320 | TGTGACGTCATC | - | 6.02 | | CTCF | MA0139.1 | chr1:40282651-40282670 | TGTCCACCAGGGGGCAGAG | + | 7.34 | | EWSR1-FLI1 | MA0149.1 | chr1:40281985-40282003 | AGGAGGAAGGAAGCAAAG | + | 6.23 | | JDP2(var.2) | MA0656.1 | chr1:40282308-40282320 | TGTGACGTCATC | - | 6.32 | | NR2F1 | MA0017.2 | chr1:40282570-40282583 | CAGAGGTCACAAG | + | 6 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_23684 | chr1:40282131-40285707 | Colon_Crypt_1 | | SE_24232 | chr1:40282541-40285645 | Colon_Crypt_2 |
|
| | 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 |
| GH01I039816 | chr1 | 40281967 | 40283916 |
|
Enhancer Sequence | TGCAGTGGGG CCTTGGAGCT CTCTTTATAT CTCACCCCTC ACCTTCTAAA TGGCAGGTTA 60
TGATTTCCTA ATATGCTGTG ACAGAGCTGA ACCCTCCATC CCAGCTGCAG GCACCTGCCT 120
CTGTGGAGTG GCTACTCTAG GCTAGGTACT TCAGCATATT CTCTCTTTTC ATCCTCCTGC 180
AGTCCAATTT GGCAGATAAG GAAACTGAGG CCTAGGGAGG TTCTGGGCTC CTGCAGAGCT 240
AGGGGAGGAG GAAGGAAGCA AAGACTAATC AGGCATCCCT TAATTGGACT TGCCTGGGAG 300
GCAGGCACTG GGCCTGAGTA GAGGGTGCTG GGAGCTGAGT GTGGTCAGAA TACAGGGAAC 360
AGAAAGGCTC AGGGTGACCA AGGCTGAATG GGGGTGGGGC AGGGTCCCTG AGGACAGGGC 420
TGAAGCACTT GGACAACTGA CTACAGTGGG GCATTTTCAG GTCTGGGCTT GTGGAGTGGA 480
CAGCTGAGGT CCCTGAGTGG GGGCACAGGA TGGCTGGAGG GGTTGGGGAG AAGGTGGTGA 540
ACCTTGGAGG AATCCAGGAG GGAGATGATG TGACGTCATC TAGGGATGCA GGGGGTGCGA 600
GAGGGGCAAG AAGCAGCAGC ACTTGGTGAC TGATGGGATA TAGAGGTTAG GGAGAAGGCG 660
GGGTGAGAGT GATGACTAAC ATTTATTGGA CACTTTGTAT GTGCGTGGCT CAGTAGCAAG 720
TGTTTCCCAT TTGTCACAGC ACTTAATCCT CAAAACATCC TAATAGTGTT GGTTCTATTG 780
TCACCCCCAT CTAACAGATG GGGACTGTGA CTCAGCGGTG AGAGTCTTAG CAGAGGTCAC 840
AAGCCAGTCC TCAAGTCCCT GGGAACCACT TGGTTCCCAC CGTCATCTCC CCCGAGATGC 900
TAGGCTGTTT GTGTCCACCA GGGGGCAGAG AGAGGCCGGG AATTTGAACG GGACCCACGT 960
TTTCCTGCGC TTCCCTTAGC CTTGGCTGTG GTCAGAGATC TTGGTGATCA AGGAGTCTGA 1020
|
