| Tag | Content |
|---|
EnhancerAtlas ID | HS146-12045 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr5:142628300-142629610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr5:142628502-142628515 | TTCTAGAACCTTC | + | 7.12 | | NFE2L1 | MA0089.2 | chr5:142628958-142628973 | CCCTGACTCAGCATT | + | 6.21 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_36001 | chr5:142628060-142630242 | HMEC | | SE_45475 | chr5:142628087-142629508 | NHLF | | SE_45680 | chr5:142627793-142629949 | Osteoblasts | | SE_55687 | chr5:142627377-142630928 | u87 | | SE_67941 | chr5:142627377-142630928 | u87 |
|
| | 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 |
| GH05I143248 | chr5 | 142628021 | 142631249 |
|
Enhancer Sequence | ACCATGGGTC TATTTCAGGT TAAAATTCAG GACTAGGAAT GGTTCATAGA AGGAAGGAGG 60
GGGATCTTTT TAAATTGACA CTCATGAGCC CCCCAGTTTG AAATGACGCC CTTGAGTTGT 120
GCCACCAAAA AGTATTTCTC TGTGTCTGCT GCAAGACCAC ATCTTCACTA CAGAGCCCAT 180
GGACTGAAAC TGTGTCCAGA GATTCTAGAA CCTTCCTGAG GCTTGAGCAC AGTGTTTGGA 240
GCAGCACTGG TAGGTGGAGA GGAGAGAGAG GAGTGAGGGA CTTGGAGGGT AGAGGGTGGT 300
GCCCCAAACA CAAAAGAAGA GATGTTCCGA CTAATGCGAG GCCTACTGTG CATGTCATTT 360
CCCTTCTTGT TCTCTCTGGT TCCCTTTCTA GGAGAATGTC TGTTCAGCTT CTGTTGAACC 420
AAACCTCCAG GTTGATTTTG GCCAGGAATC CCCACTGGGG ATTCCTGGTG GAGGGCTGTG 480
AACTTGCTGA GGATATGAAG ATATCTGAAG TCAATCAATC AGATTGCAAC ATGACACTTT 540
TTATCTTTTT AACCTAACTG CCAGCTGGAA ACTTGGAAAT CCTCCCTCAG TTTTTGCTTA 600
TTATGGGAGA CTGACTCATG GACATTAACT TGCTTCCAGC CCTTTCTAGC CCTACCCTCC 660
CTGACTCAGC ATTTTAGTAT CACAAAGAAG TCCAGAAGTC ATGTCCTTGG TGACTGTTGA 720
AGCTGAAGCA CAAAGAAGTG AAGTGACTGA CCCAACTATC TATAACCAGG AGCAGCAGAG 780
CCTGGGTTAC ACATCCATTC ACCCATAGGT GCATGCATGA GACTCATTCA ACACACACTT 840
ATTAGCATCT ACCAGGTTCC AGGCGATATG CTAACTCCTG GGGCTACAGA GTTATAATTA 900
AGATAGACCC TCTTCCTGCT CTGTTAACAC TCATGGTCCT GTAGAGAAGA TAGTCATGAA 960
AGGAATTATT TGCATTTGTA AAATGTGCAC AAATAAAGAA ATTAACAAAA ATGAAAGATG 1020
TGAGAGCTGT GAAGGAGATA TTCATGGTGC CATGAGAGTG TGGGGGGTGG GTCAGAGACT 1080
GCTCCAAAGG GGAGCTGCAT TTCAGCTGTG ACCTAAAGAT GTCTCCATCC ATGAAGAGGC 1140
TTATTGCTGA GGTGCCCTCT TCCCTTGGAC CAGAAAAGTA GGACAAAAAA CCATTCCTCT 1200
CACTGACCAC TCCAGACTTA AACAATGAAT GAGAAAATTC CCTGGCAAGA CAGGTAGCTA 1260
GCCATGTCCT GCTGAAGAAG CCTAATAGAG GGACTTTCCT GGCCCAGGAA 1310
|
