| Tag | Content |
|---|
EnhancerAtlas ID | HS101-09673 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:7736010-7737760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr12:7736889-7736900 | CTGAGTCACCC | - | 6.02 | | FOSL2 | MA0478.1 | chr12:7736918-7736929 | CTGAGTCACCC | - | 6.02 | | FOSL2 | MA0478.1 | chr12:7736947-7736958 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr12:7736889-7736900 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr12:7736918-7736929 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr12:7736947-7736958 | CTGAGTCATCC | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 7736865 | 7736957 | | chr12 | 7737079 | 7737630 | | chr12 | 7736832 | 7737158 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I007584 | chr12 | 7736832 | 7737158 |
|
Enhancer Sequence | GAGAGATGAA GCAGGCATAG ATCCTGGGAA CTTTGACCAT GCATCAGCTC CAAGGGAGCC 60
CGGCCATAAG CACTCACCCC GCAGGGCTGC CTGTCTCCCT CCCTTTGAGA GGCCCTGGCC 120
CCAGCTAACT GCTAGAGGAA AAGCAGGGAC TGCTTCTCTG CGGAACTGGG GCACATCTAT 180
CCTGCAGGCC TACTTGCCCA CTTGCCTGGC TGTCCTGTAG GAGTGTGTAC ACAGTACAGC 240
CTCTGCTGCC CAGCCTGAGT GCTTTGCTCC ACCTAAGTGC ATTCTTTCAG CCTAGGAGCG 300
CTTCAGCTCC CACAACGCGG CAGAACCCAC CCCCCAGCAT CTGGAGGAGG GAGCACCATC 360
AAGTCCTGGT ATCCCAGAAC AGCAGCCTGC AGCTCAGTAA TGCCAAGCTG GGATCTGTGG 420
TCAGCACTTA AACAGGGGAG AAGCCCAGAC TCTCAGAAAA CTGTGAAGGC TGAGTTTAAC 480
ATGTTTATGG GCTGGCATGG GACCTAGCTG TGTCTCCCTC CACAGGGCTG GTCTAGTAAA 540
GGTGTGGCCT ATTTCCTGAT CAGACCTCTC CCCAAGGGAG CCCCATGGCC AGAATGACCT 600
ATCAACTGTA GCATATAATA AATTCCTCTT CAAATGTTTT AGCCTGTCAA TTGTTAAGTA 660
CAATTAGTTC TGAGATCCTC TCCAAAGAAC CAATGTATCA GTATGTTCAG CTCCCCTGTT 720
CTTTGATCCG CATTTTAAAG TTTAAGTTCC TCATTCTCTT CATCTCCTTG CCCCTAGTTT 780
CAGTAAACAA CACCCTCCTA TCCTCTATCA CCTGCTGCAT CCTGAGTCAC CTCTGGTCAC 840
CTGCTCCATC CTAAGTCACC CCTGGTCACC TGCTCCATCC TGAGTCACCC CTGGTCACCT 900
GCTCCATCCT GAGTCACCCC TGGTCACCTG CTCTGACCTG AGTCATCCTG AGTCACCTGT 960
TCTGTAAGCA TCCTTCTTGC CAAACTACTC ACTCTGCCAC TCTGGCTCAT ACCCCTGCTC 1020
TCTTTAAAAT AGCCATTCAG AATTAGCTTA GACTGTGCAG TCCAACCCTA GCCAATAGGG 1080
AACAATGAAG CAGTAGGGGC TACCTGCATC AGGGATAAGA ACCCCTTCCC CTCCCTTGTT 1140
CAATATGATC ATCACCATGG GACCTAGTAA ACAGATTCTC CAAGGTCAAT GCAAAAAAAA 1200
AATATCTTAA AGACAGCTAG AGAGAAGGGC CAGGTTACTT AAGAGGAAAC TTCATCAAGC 1260
AGCAGCAGAC TTCTCAGGAG AAACCTTACA CATCAGAAGA GATTGGGGAC AGACTTTCAA 1320
CATCATTGAA GTAAAGAAAT TTGAACAAAA ACGTTTATAT CCTGCCTAGC CGAGATTCAT 1380
AATTAAAGGA GAAATAAAAT CCTTCTCAGA CAAGTAAGTG CTGAGGGAAT ACATTTCAAT 1440
AGGACCAGCC TTAGAGGAGG TTCTTAAGAA AGTGCTAAAC ATAGATTTGA AAGAATAACA 1500
CCTACTACCA TAATAGCACA CTTAAGCACA TAACCCACAG GCACTATAAA GCAATTACAC 1560
AATGAAGTCT ACATAACGAC CAGCTAACAA TATGATGACA GGATCAAAAT CACACATTTC 1620
AATAGTAACT TTAAATATAA GTGAGGTAAA TGACCCATTT AAAAGACCCA GAGTGGCAGA 1680
CTGGATAAAA AGACATGACC CAACCATCTG TTGTCTTCAA GAGACCCATC TCACATGTAA 1740
CAATACCCAC 1750
|
