| Tag | Content |
|---|
EnhancerAtlas ID | HS156-05347 |
Organism | Homo sapiens |
Tissue/cell | P493-6 |
Coordinate | chr17:42797780-42798960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid5a | MA0602.1 | chr17:42798004-42798018 | TTAATATTGCTATA | + | 6.1 | | MEF2A | MA0052.3 | chr17:42798757-42798769 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr17:42798757-42798769 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr17:42798756-42798771 | TTCTATTTTTAGTAG | - | 6.57 |
|
| | 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 |
| GH17I044720 | chr17 | 42797981 | 42798248 |
|
Enhancer Sequence | CATAGCAGAT CGGGAATATC TGCAATTCCT CTGACAAGGA CAGGATTGCA GCTGCAATGG 60
GGCTTCCCTG TCTTAGACGT TTTAGCCTTG AGGTTGCCCC TTTTCACCTT GCCACCAACA 120
TCAGCTTTCT TGGCCTTAGG TTTCTTCTCT TTAGTATCTG GCTTCTCAGC TTTCTCACCC 180
ATCATCTTGC AAGATGGGAA AGACTCCACT TTTTGGCTAT ATGATTAATA TTGCTATAAG 240
CATTCATTTA CAAGTTTTCA TGTGGCTGTG TTTTCATTTC TCAAGGATAT ACCTAGGAGT 300
AAAATTGCTG GGTCATACGG TAACTCTGTG TTTAACCTTT TGAGAAACTA ACACATGGTT 360
TTCCAATGTG ACTGCACGAT TCCACATTCC CTCCAGAAGT ATATGAGGGT TCCAGTTTCT 420
CATATCCTCA CCAACACTTG CTATTATCTG GCTTTTTTTT TTTTTTAAGT CAATCTCGCT 480
TGGTTTCCCA GGCTTGAATG CAGTAGTGTA ATCTTAACTC TTAACTCACT GTAACCTCCA 540
CCTCCTGGGT TCAAACAATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA TTACAGGCGT 600
GAACCACCAC GCCCGGTTAT TTTTTGTATT TTTAGTGGAG ACGGGGTTTC ACCATGTTGG 660
CCAGGCTGGT CTCGAAGTCC TTATCTCAAG TGATCCACCT GCCTCAGCCT CCCAAAGTAC 720
TGGGATACAG GTGTGAAACA CAGCACCTGG CCAAGATTTT AAAAATACTA TGTTTTTCAT 780
GTCCATTATC TCCAACTAAT TCTTCCCCCC CCCTCCCCTT TTTTGCGACA GAATCTCCCT 840
CTGTTACCCA GACTGGAGTG CAGTGGCATG ATCTCAGCTC ACTGCAACAT CTGTCTCCCA 900
GGATCATGCA ATTCTTGTGC CTCAGCCACC CAAGTAGCTG GGATTACAGG TGTGTACCAC 960
CATGCCCAGC TAATTTTTCT ATTTTTAGTA GAGGCAGGGT TTTGCCATGT TGCCCAGGCT 1020
GGTCTCGAAC TCCTGGCCTC AAGTAATGTG CCCACCTCGG CTTCCCAGAG TGCTGGGATT 1080
ACAGGTATGA GCCACTGTGC CCGGCCTAAT TCTTTTCTTT AACTGCTGTT CCTGCTTTAT 1140
GTTTTCCTGT ATCCTCCCTA GCCTTTTTGA GGATATTTAT 1180
|
