| Tag | Content |
|---|
EnhancerAtlas ID | HS052-36117 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr7:148941750-148943120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr7:148942531-148942542 | GGTGACTCATG | + | 6.62 | | FOSL2 | MA0478.1 | chr7:148942530-148942541 | GGGTGACTCAT | + | 6.14 | | JUNB | MA0490.1 | chr7:148942530-148942541 | GGGTGACTCAT | + | 6.32 | | JUND | MA0491.1 | chr7:148942531-148942542 | GGTGACTCATG | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr7 | 148941826 | 148942200 | | chr7 | 148942200 | 148943000 | | chr7 | 148943000 | 148943067 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I149245 | chr7 | 148942521 | 148942670 |
|
Enhancer Sequence | GTGTAGAGAC AAAATGAAAA CAAAAGAGAG GAGGCAAAAA TAAAAACCTA TTGGGAATGA 60
AAATGTGTGC ATTCCCATGT CTATTGGTTG ATGCTGGTGT GTAGACTGAG ATTGTAGGTA 120
AGGCCGTTGA ACAGAACACT TCATGCACCC TCTTCATGTG GCTTGGGATT TCTCAAGGGA 180
TTCTAGCACC TGGCTGCCTG TGATTTGCCC CACTTGACAG AGAGTGGAGC AGAGACGAAC 240
CATCCATGTG CCACCCTCCT TTAACTGCAG ATTCACATGC AAAGTAGATG ATGATGTCTT 300
AAGCCACTAA ATTTGGGGAT TATTTGTCAT ACAGGAGTTG ATGGTTGGAA TAGATACCTA 360
GGGAAAATGT TAAAACATTG AAAGATATTA AAAATGGAGT CTCAAAAGGC TGGGCATGGT 420
GGCTCATGCC TATAATCCTA GCACTTTGGG AGGCTGAGGC AGGTGGATCA TTTGAGGTCA 480
GGAGTTTGAG ACCCGCCTGG GCAACATGGT GAAACCCTGT CCCTACTAAA AATACAGAAA 540
AATTAACCAG GAGTGGTGGC ACACACCTGT AATCCCAGCT ACTTGGGAGG CTGAGGCAGG 600
AGAATCACTT GAACCTGAGA CAGAGGTTGC AGTAAGCTGA GATCATGCCA CTGCACTCCA 660
GCCTGCAGCC TGGGCGACAG AGCGAGAGAC TCCATCTCAG AAAAAAAAAA AAAAAAAGGA 720
TTTGCATACT ATGTTTATGA ATTGAAATTC ATCCTAAATG TGTCACTTTT CTGTTGGGTG 780
GGGTGACTCA TGCCTGTAAT ACCAGGACGT ATAATCGTGC CACTGCCCTC CAGCCTGGGT 840
GACAGAGTGA GACCGTGTCT TTATTTATTT GAGACAGAAT CTCTCTCTGT CACTGGAGGG 900
AAGTGGTGTG ATCATGGCTT CCTGCAGCCT CAATCCCCTG GGCTCAAGTG ATCTTCCCAC 960
CTCAGCTTCC TGAGTGGCTG GAACTATAGG CACCTGTCAT CATGCCTGGC TAATTTTATT 1020
GTCTTTTTGT AGAGATGGGA TTTCACCATC TTGCCCTGGC TGTTCTTGAA CTCCTGGGCT 1080
CAAGCTGTCC TCCCGCCTCA AGCCTCCCGA AGTGCTGGGA TTACAGACTC GAGCCACTGT 1140
GCCCAGCCAT AGATTCCCCA AGTGGGATTG CTAGGTAAAA GGGTTTTTAA TGACTTGAAA 1200
TTTTTCTTCC CCTAAGAGTG TGTAGTATTT TTCATTCCTT CCAGGAGTGT TATGAGAGTC 1260
AGTTTACCAC ATTATAGTCA GCTCTGAATG TTATTCTTTG TGTCTGTTTC ATGTTTGTCA 1320
GTCTGATGGG TGAACGTGCT TTCACTTAGT TATATTTGGA TTCCTGATTG 1370
|
