| Tag | Content |
|---|
EnhancerAtlas ID | HS176-37475 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:76234710-76235830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr7:76235762-76235774 | AAGTAAACAGAT | + | 6.74 | | FOXP2 | MA0593.1 | chr7:76235762-76235773 | AAGTAAACAGA | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr7:76234984-76234999 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr7:76234732-76234747 | GAGGTCAAGAGTTCA | + | 7.64 | | RARA | MA0729.1 | chr7:76234732-76234750 | GAGGTCAAGAGTTCAAGG | + | 7.63 | | SPI1 | MA0080.4 | chr7:76235520-76235534 | CACTTCCTCTTTCT | - | 6.51 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_00592 | chr7:76234056-76240067 | Adipose_Nuclei | | SE_36622 | chr7:76234572-76239823 | HMEC | | SE_55997 | chr7:76234590-76237294 | 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 |
| GH07I076605 | chr7 | 76234319 | 76237516 |
|
Enhancer Sequence | GAGGCCGAGG GGGGCGAATC ACGAGGTCAA GAGTTCAAGG TGACTATAGG GAGAAAAATT 60
ATATTTCAAT AGAAAAACGA TAGTTTACCT GTTATTATAG TAATGTTCAT TGTTTGAGTT 120
ATTTATCTAC CTGTAGACTG GATTAGATTC TAGATTCTTC CAGTTTTCTC TAATGTCTGG 180
CTACAATCTC CAGTGAAGAA TGAGAACTGG CTGGGCGCGG TGGCTCATGC CTGTAATCCC 240
AACATTTTGG TAGGCCGAGG CAGGAGGAGC ACTTGAGGTC AGGAGTTCAA GACCAGCCTG 300
GCCAACATGG TGAAACCCCG TCTGTACTAA AAAAATAAAA TAAAATTAGC TGGGCATGGT 360
GGCATGCCCC TGTAATCCCA GCTACTTGGG AGGCTGAGGT GGGAGGATGG TTTGAACCAG 420
AGAAGTCGAG GTTGCAGTGA GTTATGGTGG TGCCACTGCA ATCCAGCCTG GGCAACAGAG 480
TGAGACCCCA TCTCAAAAAA TAAACCCACA CCCAAAGTGT TGGTTTACAG AGGCTTTCCA 540
ATGCAATAGG AAGCTTCTGG AAACTTTAGG GAAAGAGGAG GATTAAGCAA TGGAGTCTAG 600
AGAACCCTCA GTGGCTTGCC ACTGCCTTTC ATTTCCAGTC TAGTTCCCCT GGGAGGCAGA 660
CAGGCCGAGC CCTCTGACAT TGCTGCTGGA GGCTGTCTCT CCTGGCAAAG GCCCAGGGAA 720
ACTATCCTGC TGAGGCCCAT CTGGAGCTGG CAGGGAGCTG ACATTCACGG CCACATCTTA 780
GTCATAACTC CTCCCCTCCC CTGACACAGC CACTTCCTCT TTCTGCTGAG AAAAGAAGTT 840
GAATGAAGGA CAAGCTCTCA GAAAGTTGCA ACCCCTAAGA ACTTGAGTAC AAGGAAGAGA 900
CGGATGTTTA TTGCAAGAAC CGTTCCCCGG TGTCTCCTGG CTCATAGAGC AGCTCCAACA 960
ACACGTGCTT GGATGCCAAG TGTGCCATGG AGACCAATCC TTGCTATAAT CCTGATGGAA 1020
AGAACTTCCC CATCTGAAAA GAGGATGGTG ATAAGTAAAC AGATTGTCAG GGGTAGAAGT 1080
ACCCGTCGGA CCCCAAGCCT GGAGCATTTT GCCAGAGACC 1120
|
