| Tag | Content |
|---|
EnhancerAtlas ID | HS118-13939 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr4:24219960-24221590 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr4:24220282-24220295 | TTCTAGAATGTTC | + | 7.34 | | MYB | MA0100.3 | chr4:24220923-24220933 | ACCAACTGTC | + | 6.02 |
| | | 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 |
| GH04I024218 | chr4 | 24220023 | 24221437 |
| Enhancer Sequence | AATGATAGCT GCAGGAAAAA AGAGATTCCA CAATGAGTTT GAAAAGCCCT GGACAAAACC 60
ATCCACACAA GTTTCTTCAC ATCTTGAAGG ATACAGAGAA ACTAGCAGGT GGATGAGGCA 120
GTCAGCGAGG AAAGACGGAG GTAGCTGTCA TCAGCAAATG CTAGCAGGAA TACAGGGCTG 180
GCCCATGATG TGGATACCCT GTGCAGACTA ATGATTTCTC ACCTTTTCAA AAAGGCATTC 240
AAATGTTGCT TAAACATTTA TTTAGAAGAG TGGCTGAGAG TTTCAGATAG GAAGGATGCA 300
GAAAGGAACA TTTTTCAATC TTTTCTAGAA TGTTCCCAGC AATTCAGCTC TGGCCCAGAC 360
TTCCATAGCC TACTCAGCAA AGCAGTTACC AGCATCCCTC CTCTTCAGGA GGTGGTTTAG 420
GAAACACCCA TTGTTGCTCA ATGTGCCTCT TGAGATGATC AGTGCTCAAG CAGCAATCAT 480
GGAGAAGATA ACCACATTTA GTCTTTTTCC TGAATAGAGT AATTTTATAT TGCTTTTTTT 540
CATCTCCAGT GACATTTCCA TGTCCCTTTG AGATTCATGC CCCAATGTCC TTGATTCTGC 600
TTTGCCTGAG ATGCACATTC ATAAGGTCAA TCCTCTCCCA GTACAATCAC CAAGTACAAG 660
GTGGGGACCA CATAAACTTC TTCAGATTAA AACAATTGTA GTGCTATTTG TGTGGGACAA 720
GAAAGAGGGG CTTATTTTCT CCCTTAGGAT TCCAAATTTT CAGCTGCTTC TGAAGTAGTG 780
GTGGCAGAAA GGTGAGTACA CAGGATAACT GGTATCCAGC CAAACCTCTT GGAGATGTTT 840
TATGGTCCCA CAACCCTTGG CAAAAGTGCC AGGAAGTCCG CTCTGCCTTT CTGCAAATGC 900
CAGCACACCA ACGGGGTGGT CACACCTGGG CCAGCAGCGT GCTTTGAACT CTTGTTATCT 960
GGCACCAACT GTCCCTGAAT CTCTCTCCAA GGCTGAGAGC AGCTGTCAGA TCAATGCCTG 1020
CAGGCTGGGA TTGCTACATT CCCGGGCCGA ATCTTACAAA CAGCAACCAG GTTATCTCCT 1080
CCGTCATACT GGGCTCTAGC TTGCCCTGAA TTCTTCAGTG AAGGAGTCAT TTTTCTGTCA 1140
CTGCCTGCGT CACTGCCTCA CCCCATGAGA GCCACCATCA AGATAAAGCC TCAGGGGAGG 1200
CGTCCTGCTC AGTTAACAAT TGATCAATCA AAGAGTTGTC TCCATTATTC TCTTAACTCT 1260
TACCTATCTT CACTAAACAC CTACAGCCAC TGGCTGGACT CCAGAGGCCC CTCCTCCCCT 1320
CCTCCAAACA TGGACGCTTC TGGTACTAGT CATAAATGTG AAGATAGGGA TGATGTTTGG 1380
ATATTTGATG ATCAGTGTGG GGTACCTCAG ACCTGGTACC GGAGGCCATA CAGACATAAG 1440
CCAACACAAA GGCCACTTCC ACATTCTGAA CTCACACCTC CACCTGCCCA TCCGTCCTGT 1500
TGAGAAGCCC CATGGAGAGA GTTCTTCCTG CTGATAATGC CTAGTCACAG AGTCCCATCA 1560
GTAAAGAGAA GTGATTTCTC TCTTTAGACA AATTTTAGAC ATAAAGTTTG AGGATTTCTC 1620
TCCTTAGGAA 1630
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