| Tag | Content |
|---|
EnhancerAtlas ID | HS052-30452 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr5:74935880-74937180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr5:74936198-74936209 | TTCTTATCTGT | + | 6.14 | | Gata1 | MA0035.3 | chr5:74936198-74936209 | TTCTTATCTGT | + | 6.62 | | HNF1A | MA0046.2 | chr5:74936663-74936678 | AATTAATGATTTACC | + | 6.68 | | HNF1B | MA0153.2 | chr5:74936664-74936677 | ATTAATGATTTAC | - | 6.67 | | NKX2-5 | MA0063.2 | chr5:74936887-74936897 | CTCAAGTGGT | - | 6.02 | | SOX10 | MA0442.2 | chr5:74936645-74936656 | TGCTTTGTTTT | - | 6.02 |
|
| | 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 |
| GH05I075639 | chr5 | 74935661 | 74937528 |
|
Enhancer Sequence | TGTTTTGAGA TGAGGTCTCA CTCTGTTGTC TAGGCTGGAG TGTGGTGATG CAATCCTATC 60
TCACTGTAGC CACAACATCC TGGGCTCAGG TGATCCTCTC ACCTCAGCCT CCTGAGTAGC 120
TGGGACTATA GGCATCCACC ACCATACTCG GTTAATTTTT TAAACTTTTT GTAGAGATGG 180
GGCTTTGCCA CGTTGCCCAG GCTGGTCTTG AACTCCTGAG CTCAAGTATT CTGCCTGCCT 240
CAGCCTCCCA AAGTGCTGGG ATTACAGGCC GAGCCACTGA ACCCAGCCAC TTTGACACTT 300
TTCAGCTGAG GTTTAGTTTT CTTATCTGTA ACATGTGGAT AATATTAACC CTGCCCTTAT 360
AGCATTGTGT GATTTAACTG TGCCAAAGCA TATAGTCTTG GCAGTACAAG TTGACACATA 420
GTTGTTCAAT AAATGCCATC CATTATTAAG AGTAATGCAC AAAAGGCATA GAGAAAGCAT 480
GTTGTTTGTC AAGTAATTTC ATTCCATGAC AAAGGGCAAT TAAATTTAAC TTATTTTTCC 540
TTTTGTTGGA ATGGAGAAAC ACCATTCTTT CTGAGTGTTG AAGGAGGTCA TGAAGAGTGC 600
AGCAAAGTGC TGCTGACAGC AGGAAGTGAC ACCAACATTC CAAATAAAGT ATGTGTTCCA 660
GACCATGTTC ACTCATGCAG TGGGAAGGAG ACTTAAAATG TTCTTTGGAA ACACTGGTCC 720
TACATTGATC CACTCACTGG TACTTTAGAA TTAATATTTA TAATATGCTT TGTTTTTGGT 780
AAGAATTAAT GATTTACCTC TAATATTCCC CAGTTACTGT GTCCTCAAAA GCAATGCCAT 840
TCTTTCTATT CTTTTGGGGA AGGAATAATT GAAAATGGGG CAAAATGAGC AAGTACTTGT 900
CACTTCTTAG AAACAGACAC TCTATTCTAC TTTGTTTTTT CATAGCAACT AGTGCACGCT 960
TGGCTTATAC AGAGAAGACG CTGAAAAAAA AGTTTATTGT GTGAAAGCTC AAGTGGTCAG 1020
CCTGGTGCAG GAAGAAGGAA GGATGGTGCC TTCCTCTAAA TGCAGAATAC TTTTGTATGT 1080
AGTCATTGTG CTAAGAACCT TTGAAACTTT TGAGACTGTG TTATTATTTT TATTTTTTTA 1140
GATCACAAAA ATAGAATTTG GAAAAGTTAA GGAAATCATT CAGAATCATA CAACTAGTCA 1200
ATAGCAGTGC AAGGATTCAA ACTAATGTCT GACACCAGTG CCTCAGCTTT TAACCCCTAC 1260
AATGGCTTTG TCTTCAGATG GTTTAGTTTC TTTTTCTGTT 1300
|
