| Tag | Content |
|---|
EnhancerAtlas ID | HS108-32393 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr5:109046610-109047970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HLTF | MA0109.1 | chr5:109047954-109047964 | AACCTTATAT | + | 6.02 | | RREB1 | MA0073.1 | chr5:109047749-109047769 | CCCCCAACCACTGCCACCCC | + | 6.15 | | SREBF1 | MA0595.1 | chr5:109047549-109047559 | ATCACCCCAC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAACTCCCGA ACTCAGGTGA TCCGCCCGCT TCGGACTCCC AAAGTGCTGG GATTACAGGC 60
GTGAGCCACC GCGCTCAGCC GCTAATTTTT GTATTTTTAG TAGAGATGGG GTTTCACCAT 120
GTTGGCCAGG CTGGTCTGGA GCTCCTGACC AGGTGATCCA CCCATCTCAG CCTACCAAAG 180
TGCTGGGATT ACAGGCATGA GCCACCGTGC CCGGACAAAA TGTGGTATCT TTAAAAGCTC 240
TGTGGTGATG GCATTTTAGA TTAAGGTAAT GTTTTATTTT ATGAAGATGT GTAGCTGTAC 300
TGCTGGCGAG ATGAATCAAC ATGTTCTAAT ACTGCTTGTA ATAAGAGTAA CTTGATTTAC 360
CATTACCTGC TGTGGTAAAT TTGTATCTTC AGTATTGGAA TTATTCAACA GAATCTATCA 420
GAAGGGATTT CAAAAGCTGC AGTCTGTGGT GTTGTGATAA GTGAAGAAAA GCATTTCCCC 480
TATTTCAGAC AGCCTTTGAT AGCATATGTA TTTAGGAAAA TATATACAGA TTCATCAACT 540
GTACCTGACT CAAATATTTT TAGCTTCTTT GGGTTGAACT TTGGGTTATG CCAAGGGATC 600
CCCTTTCGTC TTTTCATGGA GAATCACTTG TAACCAATGT TGATGTGCAC TTACAAAGAA 660
GGGTGTAAAG GTTTATAGGA CGATACTACT CGACAGCTCT GAGGATCTGG AATCTACATG 720
GTTCAACTAG CTTCTCTATT TGAGCCCTGA ACTAGTGTTG CACTCATCTC CCATTTCCTT 780
TGCTTTGCCA TTTCCAGTTG TAAAGTGATG TGTGCTCCCT CTCTTGCCTT TCACTGGTGC 840
AGTGGGGCTT GTCTTTCAGG ATGGGACCTG TGCTAAAACT TTTTCTTGTC TCTGTGTATG 900
CTGATAAACA GGCTTTAGAG TTCTATCTTG TGGTGACTTA TCACCCCACC CCATCTTAGA 960
GATGACAATT GCCTTTAAAG GACTATAGTT TTAATGTGTA GAGGGGCTCT TTCTGTTATG 1020
TGCTTCTAAG TAGAGAGGCC TGTGAGAGCA TCTTTCAGGT CTGAGAAGGT ACATGGCTGT 1080
CTTGTGCTCC TTTCTTCTCT AGCATCAGGC TGTAGATATT CACCCCTAGT GTTGTATTGC 1140
CCCCAACCAC TGCCACCCCC AGTGATTTGC TGCTAATTTT GGCTACTTTT TTTTTTTTTT 1200
TAATTCCAAA ATCTGTTGCA GTCTCTTCGG ACTTCTGCCA ATTCTGGCAT AGTTTGCTCA 1260
AATGATTGGC CTTTTCTTGG TAGATCTCAG TCTCTTAACT TCTCCCTTTC CCCTTGTTGA 1320
ACTGACCAAT AACCTGTGAG TATAAACCTT ATATCTTGTG 1360
|
| |
|
|
|
