| Tag | Content |
|---|
EnhancerAtlas ID | HS040-10209 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr14:59658370-59659870 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr14:59658752-59658763 | AGAGGGTGTGG | - | 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 |
| GH14I059192 | chr14 | 59658719 | 59659190 |
|
Enhancer Sequence | ACATCGACTG TTTCTTTGTA GTTACAATTT CTTATTACCC CTGAACCAGG CATTTCTAGA 60
TTTCTCTCAG TTGCACTATC CTTGGCCCAG ATAATCTTCC CAGGAGGTGT GTGACACGTG 120
AATAGGGAGA GACACCAAGA GAAAGATACC CAGAAGCCTT TGCCAGGCCA CCAGTGTCTC 180
CCAGAAGAGC TGGGAGACAA TAGTCCTCTC ACCTGAGGCA GAGCCGTTCC GTAAACAGGA 240
TCAGTTGTTT CAGGCTGGTT GATGTGAAAG AAATGTGAAA GAACATTTGC CCAATATTTG 300
TAACATGTTA CCATCCAGTA GTCTGATTCT GTGGGTTTTC AGGAGCATAA ATTAGTAAAT 360
TAGTGAGGAG GTGTGATAAT GAAGAGGGTG TGGTGGGTCA CATCCTTGGG TGGTGCTTAC 420
AGGAGCTCCA TGAATAGGTG CTAAGGAATT TGAATCCTGG CTTTCTTGTT TTGTGGACAT 480
GTTCTGCTTG TTAAGGGGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 540
TGGTTTTGAG CTACTTTGTT TAAAAGGCTG CTTTTAGTGT TGGCACTATG GTCCTTAAAA 600
CAAATAAGGT GTTTACAAGC AAAAGTTCTG ATTGAAAGTG TTTCATTTTG TAAATATTTG 660
GGAGATGGCA TAAAGAGAAA CTTGAGGTCT TGTGTGAAAA CACTTTAAAG TTGCAGCTGT 720
TGGACCAGAG GAAACATGCT TTTCCAACAA AGCTTGGTAT CCTTGAGTGC CCTAGGTGTT 780
TGGTTCAGGA AATAATCACA GAGCTTGTAA CTGCTGTGGG GCCCTCCCTG GCTTCAAGCC 840
GTGCTCTGGT ATTTCCAGTG TTAAGTCTAT CCTTATATTG CCGGAAACAA AGCAAGGTGT 900
CCAACTTGGG TTAGCAAACT TGTTTTCTCT CTAGAGGGGA CACCAGTCAA AATAGAAGTT 960
CTATATTCTG TTGTGATTTT TTCCTCTTTG GATGAGGAAT ATGGTGACTT ATTTTGGTAT 1020
TACAATTTCT AACTTGGTAA TAGAGGTAAT ATTCTAAGTG AATACCAATC TTAAGTACGC 1080
ACAGCATCTG TTGTAGTGGT TTCAAGACCT CAAAGTTTAG GCCGGGCGCG GTGGCTCAAG 1140
CCTGTAATCC CAGCACTTTG GGAGGCCAAG TCGGGAGGAT CATGAGGTCA GGACATCGAG 1200
ACCATCCTGG CTAACACGGG GAAACCCCGT CTCTACTAAA AATACAAAAA ATTAGCCGGG 1260
TGTGGTGGCG GGTGCCTGTA GTCCCAGTTA CTCAGGAGGC TGAGGCAGGA GAATGTCCTG 1320
AACCAGGGAG GCGGAGCTTG CAGTGAACGG AGATTGCGCC ACTGAACTCC AGCCTGGACT 1380
ACAGAGCGAG ACTCCGTCTC AAAACAACAA CAACAACAAC AACAACAAAA CCCTCAAAGT 1440
TTAGAGGAAA TTGATTGCAC AGGTACTATT TAAGAAACTG GTACTGAGAG CATTTTCTCT 1500
|
