| Tag | Content |
|---|
EnhancerAtlas ID | HS176-12050 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:111292340-111293750 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr13:111292423-111292434 | GGGAGATAAGA | - | 6.62 | | NFE2L1 | MA0089.2 | chr13:111293051-111293066 | CCTGCTGAGTCACTG | - | 6.14 | | Nfe2l2 | MA0150.2 | chr13:111293053-111293068 | TGCTGAGTCACTGAC | - | 6 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09490 | chr13:111292213-111293723 | CD14 | | SE_55064 | chr13:111292408-111294399 | Stomach_Smooth_Muscle | | SE_65828 | chr13:111292403-111294485 | Pancreatic_islets |
|
| | 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 |
| GH13I110640 | chr13 | 111292902 | 111294139 |
|
Enhancer Sequence | AAATTGAGTA TTGTATTTTT TTCCTTAAAC AGCTAAAGCT CACCTTTCAA CTTTCTTAGG 60
TGAGGACATT GTGTGAGATG CCAGGGAGAT AAGAATATCT AAGCCTGTCT GTGTGAGATT 120
GGCCTCCTCG CCAGCGCCTC TCCCGTGGTG GCTGCAATAA AGCACCTTGA AGGATAAGCC 180
CAAGGCAGCC CCTTCTTTCC TTAGGAAATA GAATTCAGCA GTCACAGGAA CTATTCGTCT 240
GGTTTTTGTT CTAAGTAAAA CATCCCTTTG CTTAAAGGAG AGAATGGGTT TTTTTACAAG 300
CAGCTCATTG CTTCCATGTT CTTTCTCAAA CCCACGTATT TCACGCACTC GCTCCAGCCG 360
GACACGCTCC CAGGAGCTTC CCTGGACCAG GAGAGCAACG GGAAAGTGTG GGGGGGTGGG 420
CGGCCCGTAA TGCCCCAGTA CTGAGCAGCC CTGTCGAGAT GCCTCATTGT AAGGAGCCCT 480
CTGGGGACTT TTTCTATGTG GGTAGCTTTA CTAGGGTGAT TTTCTAGGTG AGTGACTTCT 540
GAACTGTAGA CAGGAGACCT GTACCTCAGG GTCACGGTTA AATGATGAGC AAGCCCGTAT 600
CCCCAGTCAC GGGTCCCGCT GCTGCCTGTG CCCTTGGGAT TCAGAGATGC CAGTGTGACA 660
GGGAGAGGCC TGGCCCAGGG TCTGCGAGCA GGAAGAGTGG AGAGGGGTCA CCCTGCTGAG 720
TCACTGACAG CTGTGGCGCT GGGCTTACCA CAGAAGGGTG AGATCAGGAG CAAGGTGGGT 780
GCTTCAGGAG GCCACCGGTC CTGTAGCCCA GGCAGCCTGC CGTGTGCTGG CCGCCACCTC 840
CCGCTCAGGA ATCCTGTCTG TCACAGCTCG CCAGCTGGCT TTCAGCCTGG CTGCCCTGAC 900
TCCTCCGGAA CCAACCTTTC CCAGGCCCAG CTCGACCCCA TCACTGCTCT GCACAGACCA 960
TGACCACCAA GATGGCCTGC AGCTGCCAGG ATGTTAACTG CAGCGGGACT GCAGACGGGT 1020
TCTCAGCTGC ATTTTTCCTA TGCTGAATAC GTTACTTTTG TAACCAGAGA GAAAACGTAA 1080
GATTGTGTTC TTGCTGGGGG AGGTGTCCCG GGGTTAGCAT TGCTGGCGTC CCACCTCTGC 1140
TTCAGACTAT GCTGCGTGGC CCACCCACCT CACCCATCCC CAGCCCCTCC CTCAGGAGGA 1200
AACAGGCTGC ATTCTGCCGC CTCCCGGGGT CCCTGCTCTT CTGTTGGCTG TGTTGTCTGT 1260
TCCCTGGGCA CAGGGCCAGC AGGTCTCACG CACAGGCACG TGTGCTGCTG GATGCTACTG 1320
AATGTCTGAC ACTACTTCAC TCAATCGACG GTGAGTCTGT AGCCACAGAA CGCAGTGAGT 1380
GTTTAGGCTC AGTTACTAAC AAACAGACGC 1410
|
