| Tag | Content |
|---|
EnhancerAtlas ID | HS007-11772 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr3:132597900-132599210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr3:132598302-132598313 | AAGCCATAAAA | + | 6.62 | | Lhx3 | MA0135.1 | chr3:132598216-132598229 | TAATTAATTAATA | + | 6.25 | | POU6F1 | MA0628.1 | chr3:132598218-132598228 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr3:132598218-132598228 | ATTAATTAAT | - | 6.02 | | RELA | MA0107.1 | chr3:132598772-132598782 | GGGAATTTCC | + | 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 |
| GH03I132879 | chr3 | 132598721 | 132598870 |
|
Enhancer Sequence | ACCTAGACAA GAACCCAGGA CATAGGGTAC TATTTCAGAG CTCTTTCCAC TGTACTATAT 60
TGCCTAGTGT TTGTGGTCAA GTATGGGGCT GTGTGTGCAC ATAGGGATGG AAAACTGTTG 120
AGATCCCAAA GAATGAATCT TAGATGGTGA AGTTCCAGCC ATATGATAAG AGTGGGATTT 180
CGTCTGTTTC TCTGCAAATA GTGCCAATAG AAATGCTACC CTGCCTAGGT TAAGGATGTG 240
TTATAGAATG TGGTTGTTAG GAAGGCTTAA GACAATAAAT GGTAAAGAAT CTGGCACAGT 300
GCCTGGCACA CAGAGGTAAT TAATTAATAA ATGAAAGTAT GATTTCTAGA GGGCCTCACG 360
CTGCGTATTT GAAGTACTCC TTCCTATTGT GGTGCCTCTG GAAAGCCATA AAACATAGTA 420
ATTATAGCTT ATACTTATAG CATAGTACAT AGAACTTATA GCTCATCTTC CTTGGGTAGC 480
CTGGGGATGC CCTGGGTTTG GAGGCCTCTC CATGAAGGGA TTTTTGGCTG GTTCTGCCAG 540
GCCCAAAGAG TTCATCTTGT AGGTCCTGTC CAATGTTTCT CAGTCATAGG TTCTGTTTTT 600
CACTAATGAT ACTTCCACCC AAGACCTGGA ACAGAAAGCT TACTTCCAAA TGCTACTTTT 660
TAGATCCAGA TTACAGATGG AGCAGAGTTT TTCTGACCCT GACATTGTGC AGAGATCTGT 720
TCTGGCTGCT TGCCTGCCTA TGTCACTCTG CTTCCTGCTT AGGCATCAAA ACCTCAGACC 780
TTAACAGGCA ACTAAGACTT ATGCCTGGAG GGCTTCACAG CTCTAACTCC CACCTGCTAT 840
ACTATCTAAA GACTCCTTTG TTTCTGATTC CTGGGAATTT CCCTTTCTTG TTTGCATGTG 900
TATTAAAGAA AAACTGCTAA GCTCTGAGCA TTCAGCCCAT TTATTGAATG ACCCCAGGCC 960
CACTGGAAAT TCACTCAACC AGTTGTGGAC TTCTTTGAAA CCAGATTTCC TTTTATTACA 1020
GAAAAGGAAA GGAAGAATTT ACATTCTGCC TCATGGGCCA ACCGGAGACC TGAACTCAGA 1080
ATCTTGCCTT CTGGGTGTAT GTCCTTCTTT TTGCCATATC CAGGTTCTTT CCATTTCTGC 1140
TTGGAGAGAC CTGCTGAAAC CACACTTGAG GGAGGCAATG TGGCTCTCCC TGACCAGGTA 1200
CAGAATAAAT CCAGCTTTGT CTCAGACCAT GTTTGGTGGT CTGTTGTTAC TGTCCAACAC 1260
AAATCTATTT TTAATTTTAA AAAAATATGA ACAAATATAG TTATATATAT 1310
|
