| Tag | Content |
|---|
EnhancerAtlas ID | HS048-25532 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr3:49302960-49305090 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr3:49304132-49304145 | TTCTAGAAGCTTC | + | 6.28 | | IRF1 | MA0050.2 | chr3:49303061-49303082 | AAAAAAAAAAAGAAAGAAAAG | - | 6.41 | | PPARG | MA0066.1 | chr3:49303473-49303493 | GTAGGTCCCAGTGCCCAACT | + | 6.97 |
|
| | 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 |
| GH03I049265 | chr3 | 49302455 | 49305072 |
|
Enhancer Sequence | CTTGATCTCC TGACCTCGTG ATCTGCCTGC CTCGGCCTCC CAAAATGCTG CGATTACAGG 60
CGTGAGCCAC CACTCCCGGC CAAGACTCTG TCTTAAAAAA AAAAAAAAAA AAGAAAGAAA 120
AGAAACAGCA CTCTAATACC AGGTGAGCCC CTGGTCTAGC CATTTCAGGA GGGAGATTGG 180
CCTGAGCTAG GCCCCTTTTG CAAATCTTCT TCACTGACCT TTGAACATTG ACAACTCACA 240
ATTTCACCAG TTGGCAGAAT GGTGTTACTT TATCACTGCA TTCCTGAGTG AAAAGGTGAG 300
GGACACAGGC CTCCAGGTTG TCTGTCTCCT TCCTTCTGGT CTGTGGATGC TGTTGGAATC 360
ATCTCTGGGA TTGAAAGAGA CGGTGGTGGG GTGGGCCCAG GAGAATGCCA AGGAATCAGG 420
GCAGGTGTGC CAGGAGTTGG CTCCCCTATC CTAAGAGTGA GGGGAGCAGC AGATAGATGG 480
GTAAGGGGAA CCCTGAGTCC TAGAGATGAG AAGGTAGGTC CCAGTGCCCA ACTGTGGTGG 540
CTTGAGCCTC ACAGAGGCAG AGGTGTGCTA ATGTAAGTGC TCCCAGAGCT CAACTGGCAA 600
GAGTTCACAA TGTAGAACCA GATCCACGTG ACTACACAGG CGTGATGCCT GTGAGTGTGG 660
GGAACACAGG AATCAGAATG AACTGAGGGC CGGGTCATTT CCAGCCTGCA GCCAGCCCTT 720
TTTAATTTCC CTTTTGAAAG AATTGCTGGC CAGGCACGGT GGCTCACGCC TGTAATCCTA 780
GCACTTTGGA AAGCCGAGGC GGGTGGATCA CGAGGTCAGG GGTTCGAGAC CAGCCTGACC 840
AACATGGTGA AACCCAGTCT CTACTAAAAA TACAAAAATT AGCCAGGCGT GGTGGCACAG 900
GCCTGTAATC CCAGCTACTC AGGAGGCTGA GGCAGGAGAA TCCCTTGAAC CTGGGAGGCG 960
GAGGTTGCAT TGAGCCGAGA TTGTGCCACT GCACTCCAGC CTGGGCAATA GACCAAGACT 1020
CTGTCTCAAA AAAAAAAGAA TTGCTGCTTT TCTCCCAGGC CTCAGCTGTG ACTCTGTGTT 1080
CCCTGCTGGA ACTTCACTCC ACCATTCACT TATCTCTCTC CTTGTTCCTG CCCTTTCTTC 1140
TCAGCCTTCC CTTCCAGCTC TTAAATCTCT CTTTCTAGAA GCTTCTAAAG ACCAGCTCCT 1200
CCCTTAAGTA TTGTTACGAA GTTTATCATC AGTTGGCTTA CAACCCTGGT TTCTACTGGC 1260
TTTGGCATGA ACACTGGTGG GATGCAGCCA TGGATCCTGG AAATCTCTTG TCATAGGGTT 1320
GGATGGGTCC ATCTTCTCAT ATGCCTTGTG CTATGGCTTG AATTTGCAGT TTGCAACTAG 1380
CAAGTTCCAA AGCTATTTAT TTTTGAAGCT GTCTTGTTTC TATTTTGATT CTGGTAATCC 1440
AAATTGCAGT TTGGTGTTTC CACGGAAACA ATTCAGTGAT TGTTTGGCTT GCCAAGATGA 1500
ACTGTGGGGG AGAGAACTGA ATGATGTAAA ATATTTAAAG TTTCTCAGTC ATGATCAAAG 1560
TCAACTATCA AGTCTCCCTG AGAAGGATTT GGTCCTAGCT CCTTAAAAAC CTGAGGAAGT 1620
TTTATTAAAA TTCTGGGCTT TTGTTCCCCC TCCAACTAAA TCCCTGGAGA ACAGCTCCCC 1680
AAACCCTGTT CTGAGCAAAT GAGCGTGTAT CTGCTCACTG TATAGACTCA GATGACGAAG 1740
GCGGGAAGTT CTTCTTGGGC ACCTCAGGGA GCCAGAGATG CAGAGACGGG AGTAGATCGT 1800
GTCACCAGGG AAATGAGGAG GCCTATGTGC CCACTCCCTG CTAATCTGGG ACTGGCATGG 1860
AGAGGCTCAG GACTCACCTG CTTGACTGTA CAGCTGCATT TCTAGTGAGG AAAAGTTCCA 1920
CATTCAAGGA TTCCAGGATG AATTGCCTGT TTGGAAAATC TGAATTTTTA AATAAAGGCT 1980
TTGCTTAAGC AAAGACATAC CTGTCTCTCT GGCCAGGGAG AGCCTGTATT CTCCCTCATT 2040
CCTCACCCCC ACCCTGTGCT GGGCCCTCAT TCCCGTCTCT ACTCCAGGTA GGAAAAATAA 2100
ATAAATTTCA AAGTCTTCTA GAGTAAGGGA 2130
|
