| Tag | Content |
|---|
EnhancerAtlas ID | HS101-28776 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr22:30433180-30435020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr22:30433783-30433794 | ATTGCACAATA | + | 6.62 | | MIXL1 | MA0662.1 | chr22:30433181-30433191 | TCTAATTAAC | + | 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 |
| GH22I030038 | chr22 | 30434052 | 30434978 |
|
Enhancer Sequence | ATCTAATTAA CATATGCGTT ACCTCACATA CTTATTTTTT TGTGATGAGA GACACTTAAA 60
ATCTACCCTC TTAGAGATTT TCAAGAATAC AATGCATTGT TATTAACTAA GTCACCTTGT 120
GGTGCAATAG AGCTCTTTAA CCTAATCCTA TTTAACTGAA ATTTATCCTT TAACCAGTAT 180
CTCCCACTGT TTTGTTTAAA AGTATGTTTT AACAAAAGGT AATTGCAACT ATAGGCTAAT 240
TCTTTGTTGT TGTTGTCGTT ATTGAGAGAG GGTCAGTCTC GCTCTGTTGC CCAGGCTGGA 300
GTGCAGTGGC ACGATCTTGG CTCACTACAA CCTCCGCCTC CTGGGTTCAA GAGATTCTCG 360
TGCCTCAGCT TCCTGAGTAG CAGGGATTAT AGGCATGCAC CAGTACACCC AGCTAATTTT 420
TGTAGTTTTA GTAGAGGTGG GGTTTTGCCA TGTTGGCTTG GCTGGTCTCA AACTTCTGAC 480
CTTAAGTGAT CCACCTGCCT TGACCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA 540
CTCCCGACCA GGCTAATTCT TAAAAATAAT ATTTTAGGTG TATTTCCCTC CCCAAATTAT 600
ATGATTGCAC AATAGGACAT TATTTCATGT TTGATTTTCT AGTGTAATCA ATCACAGGAT 660
CATTTTAGGA AAAGTTAGTC AAGGGCTTCC TCAATTTCCC TCTTAAATCC TTTAGTCTTT 720
GATATTCACA TCATCCCCCT AGGAAACACC TAATTGGTTA GACATGTCAC CTTCCCCTTC 780
ATTTGTTAAT GGACCTACTC TCTGCGATCC TTATTTCCAA TGGCTACACT CATCTGAGCA 840
GTTTGCCAAC ACATTCACCA ACTATGTGAA ATTCTGCATA TTTTACAAAA CTTAAATTGT 900
ACTTTGGTGC CTGTTTTGTT GTATTTTCAA CATCTCACAA TCCGTAACAG GGAAGTTGGG 960
CTATGGTGGA TGGAGAGTAT GTTAAGGAGG AAGAGATGTT TAAGTGGAGA GTGATTTTTC 1020
TAAGTGGTTG AGTTGTGTAG AGAATACTCT TCATGTCTGA TGACTTTAGC TTTCTCCACA 1080
ACTAGTGGCT ACAGGAACTT GGATACTGAC TAGTTGGAGT TATAGCTCAG AGGAAGAAGA 1140
GAGTACATGT ACATCTGAGC AGGGAGCCTG CCCCTTGGGG GATAGCAGTG ACATCAACAC 1200
ATGGCAATAT GATGACGTCA AGGTGAGCCA AGGCAAGTGG GCGGGTTTCA GGATCTGAGC 1260
CAGAGGGCAT GGGTTAGCGA ACAGGAAAGG CAGGAAATAT TTGTTAAAAG CTTAGGCCAA 1320
AAAAGTCTCC TATGTCAGGC CAAACACTGG TCCCAATTCT ATAGGTATTT GAGGTTTCTG 1380
AACAGAGAAT GGAACAAGAT GATAATAGTT AATATTTGTT ATGGGCTAGG CACTGTCCAA 1440
ATACTTTCCA TGAGTAACAC ATTTAATTCT CCTATTAACC TGGTGAGGTA CTGTGACAGC 1500
CTCATTTGAA ACTAAGATGA CTGAGCCAGT AGAGCTGTTA AGCCCCTTGC CCAAGGTCAC 1560
CCAGAAAGTT GAAGCAGCTG AGCCATGGTT TGAATCTGGC CCCTCTGCCT CCTGAAATCA 1620
CGCTCTCAAC CGCTGCGCTA CCCAGTCTCT CCTGGGCCCA GGATGAATGG AAGTGGGTGC 1680
TGGGAGGCGA GGCAAGATGA GGTGGAAAGA GCAGTAAGAG GCCACCTGCA TGAAAAAGGC 1740
CTAAACCAGG GCAGAGAAGG GTTCAAGAGC AACTCCAAAG AACACTGAAT GTTAAAGTAC 1800
TAGTGCTGTT TCATTGGCTT TACACAGGAC TGTTTCTTTC 1840
|
