| Tag | Content |
|---|
EnhancerAtlas ID | HS098-54676 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr8:38406230-38407650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr8:38406640-38406661 | AAAAAAAAAGAAAAAGAAAAA | - | 6.09 | | IRF1 | MA0050.2 | chr8:38406646-38406667 | AAAGAAAAAGAAAAAGAAAAA | - | 6.17 | | IRF1 | MA0050.2 | chr8:38407038-38407059 | TAATAGAAACAGAAACAAAAA | - | 6.24 | | JUN(var.2) | MA0489.1 | chr8:38406973-38406987 | ATGACTCATCTCCA | - | 6.11 | | JUN(var.2) | MA0489.1 | chr8:38406968-38406982 | AGAAAATGACTCAT | + | 7.64 |
|
| | 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 |
| GH08I038549 | chr8 | 38406722 | 38407104 |
|
Enhancer Sequence | ATACTGTGAT CTTTTCTTCC TGTTTTACAA CTCTTTATTT TTTGGGTCCA TTTTATGTGG 60
AAGGGTAGTA TAGCTTCAAA TACAGCCATT TGCTTTTATC AGTAAAGAAC ACAGAAACTA 120
CTCTAGGGCC AGGCACTGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCA 180
GGTGGATCAC GAGGTCAGGA GATTGAGACC ATCCTGGCTA ACACGGTGAA ACCCCATCTC 240
TACTAAAAAT ACAAAAAATT AGCCAGGCCT GGTGGCAGGC ACCTGTAGTC CTAGCTACTC 300
GGGAGGCTGA GACAGGAGAA TGGTGTGAAC GCAGGAGGCG GAGCTTGCAG TGAGCCAAGA 360
TCACGCCACT GCACTCCAGC CTGGGCGACA GAGCCAGACT CCGTCTCAAA AAAAAAAAAG 420
AAAAAGAAAA AGAAAAAAGA AACTATTCTA GGTATTTCAA GCAGAAAGGG ATCAAATATA 480
GGGAATTGGG TGCTAACAAA AAGAAAATCA GGGGATGCAT GTAACTTTCA GATTGACCAC 540
TGTAGCTATA GTCCAGAGAG TCTAGAAGTT GCTGTTATCA TCTATTAATA GATGTCAGAG 600
AACTGGAGGA AATCTCTGCT GGTATCACAC TTATCCTGCA TCCCTGGGGT CCATGGGTGG 660
CAGGGGAATG GAGTCTAGCC AGACTCTACA TAAACTATGT CTGACCGAGT CTAGACACCC 720
ACTGCCTCTG CTGGAGGAAG AAAATGACTC ATCTCCAATC TCCCTTCCAA ATCTCTGGTA 780
CAAAGTTTAG AAGAGGGTAG CAAGACGCTA ATAGAAACAG AAACAAAAAA TAAAAATAAA 840
TACACAAAGC TAGCTTCTCT ACTGTCCTCT TCTAGATCTC TCTTAGGCTA GAGTCTCTTA 900
ATCTACTTAT GTCTTGTCTT TCATATTTTT CCTTCTTTTC CTCTTTGTAT TTCATTTTGG 960
ATAAATTTTT CCATACTATC CCCCATTTCA TCATTTTTTC TCTGACTACA CTCAGTCTAG 1020
AGTTTAACCT GAATATTGAG GCTTAAACAA TTCAATGGCT ATTTTTTGTG TCTAAGATTT 1080
CCAGTTTGTT CGTTTTCCTT GAGTTTTTTT TTTTTTTTTT TTGACAGAGT CTCACTCTGT 1140
CACCCAGGCT AGAGTGCAGT GGTGTGATCT CGGCTCACTG CAACCTCCAC CTCCCAGGTT 1200
CAAGCAATTC TCCTGCCTCA GCCTCCTGAG TAGCTAGGAT TACAGGCATG CGCCACCACG 1260
CCTGGCTAAT TTTGTATTTT TAGAAGAGAC AGTGTTTCAC CATGTTAGCC AGGGTGGTCT 1320
CAAACTCCTG ACCTCAGGTG ATCCACCTGC CTTGGCCTCC CAAAGTGCTG GGATTACAGG 1380
CATGAGCCAT CGTGCCCAGG CTTTTCCTAA TCTTTTTTTT 1420
|
