| Tag | Content |
|---|
EnhancerAtlas ID | HS108-32616 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr5:131658050-131659490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr5:131659154-131659166 | TGCTGTGATTTA | - | 6.27 | | GLI2 | MA0734.2 | chr5:131658196-131658211 | CATTGTGGGTGGGCC | - | 6.37 | | Gfi1b | MA0483.1 | chr5:131659154-131659165 | TGCTGTGATTT | - | 6.62 | | Myog | MA0500.1 | chr5:131659043-131659054 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chr5:131659043-131659054 | CTGCAGCTGTT | - | 6.62 |
|
| | 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 |
| GH05I132322 | chr5 | 131657861 | 131658750 |
|
Enhancer Sequence | GAGTGTGACT CGTCCCCAGA CAGGCCCTCT GCTGTGGGTC AGCACACCTG GAACACACCT 60
GGAGCCTGAT GCTGACCTAG CCTGGGCTTG CATGACCTCC ACGGAACTCG CGGAGGCCAG 120
CTTCCAAGCC GGGAGAGTTT TTGCCTCATT GTGGGTGGGC CTGTGTGCTG GAGTTTGAGT 180
CTCCATTGTC CTAAAAAGCA CATTCTCAGG ATTCCAATCT CTTCCTTGAT ACCAGCCACT 240
CCTGTCTGTT GCTACTTGTT ATTTGTGGAG CTGGTGGTGT TGGATTTTGT TGTTTTTAAC 300
TCTGCCCCCT GCTCTTTCAT CACTTTTCTC TCTCTAGAAA AATCTCACTC TATCCAACTA 360
ATGTAATTCT TCAAGCTTCC CTATCATATA ACGATTAGCA TCTATGAAAG GGAAGCCTAT 420
TTATTAGCAC TATGATAGTG TGCCTATTTA TCTGCTATGT CTCGAAGAGT GAGAAAATTA 480
CTTTTTATTT AATAAATTGT TAGAGAAATG TCCTCTTCTC TCCTCCCACA ACCTCCCAAC 540
TCAGTTTTAA CACAACAGTT ATAGGAATAA CAAAGTTTGA AGATTCTGGC CTCAGTCTTG 600
CCCAATATGA CTATCTGGGG GATTTCAGGT GAAAGAATAA ATTAAAAATC ATAGAACAAG 660
GTGTCAGACA TACCCTCTTT TTGGAGATTT CCTGTTCCTT TGCTTTTTCA TATTTAAGCA 720
AGAGAAAAGG AGATTCCTTC CATTGGTGGG TCTGGTTCTG TCTCTCTCTC ATTCTCTTTC 780
TCTCTCATTA ATTCTTCTTT GTTTGATTTC ATTATATCAA AGTCAAATCT TCCAGCACTG 840
ACTGGTTTCA CCGAACTGCA TAACTTCTAC CTGCTTACAC ATAACACAAG CTTCTTTGAC 900
CATTTTTTGG AACTCACAAT TTAGACTAGA CCTCATGGTT GCCCTGTCCT TTGGATACCT 960
CCTGACTGGG AAGCTGTCTA GGCCTTTATC TTACTGCAGC TGTTAGGCAG TCATAGAGGT 1020
TGACAGGCAG GCCACCTGTC TGACGAGATA GCGCAGGTCA GGTGGGCTCA CTCTAAGCCC 1080
CTGTATTCTC ATGACCTGTA AGAGTGCTGT GATTTACTAG TGTAAATTAT TGGCATGAAG 1140
TGTGCAGGGG GAGTTGACAG TTTGTTAAAG GTTATGTATT ATTCTGATTT GCAACATTCC 1200
TCTGGAACCC TGTCTGAGGA CCGGGAAACC CGGCCTGAGG AGCAGTGAAT AAGGGCTGGC 1260
CATTATCTAC ATAGCTGTGC CTCCAAGGAA AGCATCCCAG ACTTACAAGA GCAGAGCAAT 1320
TTTCTGAATG AGAGTAATTA TCATCATCAT CATCTGTCCT TCTCTCCACA ACTCCCTTGC 1380
TAGCTGAATT TATTGGAAAA GATGTTAGTG ACTAAGGTTC TCTCAAGACA CATGACAAGA 1440
|
