| Tag | Content |
|---|
EnhancerAtlas ID | HS040-01630 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:47943100-47944290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr1:47943320-47943337 | GCAAGTCCCGCCCTCTT | + | 6.38 |
| | | 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 |
| GH01I047477 | chr1 | 47942901 | 47944366 |
| Enhancer Sequence | ATAATCCATG ATAATCTCTC CATCTGAGAT CCTTCATTTA ATCACATCTG CAAAGTCCCT 60
TTCACCATGT AAGGTAACAT ATTCACAGAC TCTGAGGATG AGGATGTGGA CATCTTGAGG 120
GTGGGGAGCA TTATTCGGCC TCCCACACCA TCTTGCAGAT GAGAAAACTA AGACTTACAA 180
AGGTCAAGGA ACTTGCCTAA AGTTCTACAG CCAGTAACTG GCAAGTCCCG CCCTCTTTGG 240
ATTTGAGCCT CCAGCTCTTA ACCTCAAACA AGAAGACTGC TGGTGCAGGT GAACCTTGAA 300
CTAGGTTTTG AAGAATGAAT CAGAGTTAAA AAAAGGTGTG TCCAGTGGAG GAATGGTGTA 360
TGCAAAAGCA AGCTGAGCAC TGGGTGTGCT TTGGTACCAT AAAATGCTCA GATTCGCTGG 420
GGGTGCAGGG AGGTGAGACA AGACAGGTAG GCAGGGTCTG GATGGTGGAA AGCCGCCTAG 480
AGCAGGCTAC AATGTTTGCA GTTGAATTGA AAGATGTGAA AAACCATTGG AGGATTTCAC 540
CTGTATGTCC TGGGTAATCC CTTCCCCTTT CTGACCCTCA GTTTCCAGCT CCTCTGCCCT 600
GATCTGCTTT TTCCCTCCCC ACTGTCCCTT TGTCCCCTCC CTTCTCACCC CCTTGCTGCC 660
AGGCCTGGTC CCATCCATCC CTGGGCAGGA ATGAGGGCTG GGTGAACTGC CCCCTTCCCC 720
CATCCCCAGG ACAGCGACGG TTTCCAAATA TCTGTCTGTT GAAATAATGT TCTCTGGGCA 780
CTGGGCCTCC CTCCCTCCCT CACATTCCTG GGCGAGCCGG CCTGTTTGGC TTGCTCGGAC 840
AAATATTGAC TTTCTCTGTC CTTCTCACTC TGGGTCTGTT TAAAAGGCAT CAATCTTTGC 900
CGGGGTGTGA GCTCCCTCTC CGTAACCTGT GGCCTCTGCG GTCCTATTCG GGCAGGGAGT 960
GGTAGGGGAG GGGCTCACAG GCTCTGGGGA TACCCCTTTC TTGCTTGGCT GCACTATAGA 1020
GGCTTTTGGT GCAATGCTGT TCCTTGTCAG CTGCTTTCCA CGCGGTCCTG CGTGGGGCCT 1080
AACAGCCCAC TTATGGAGCC TCTACTTGAG GGTCAGGTCT ATGCCCGTGG CATGTGCACT 1140
GAGACCTTCA TACACATTTC TCTAGACTCC TCAATAACCA GGCAGGAAAC 1190
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