| Tag | Content |
|---|
EnhancerAtlas ID | HS007-02956 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr11:64139690-64141160 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr11:64141059-64141070 | GGGCAGGTGGG | - | 6.14 |
| | | 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 |
| GH11I064372 | chr11 | 64140220 | 64141555 |
| Enhancer Sequence | GCGTGTCCTC GTTCGTGTTG TGGGTGTCTA GAGCAGAGAT TCTGGGCAGA CAGGCTGCTA 60
GCCCGTGGAG TTTGGAACCT CAGTGGGGAG GGACAGGCAG ACTCTTCTGG GCAAGAAGAT 120
ATTCTTTGTT CCTTGACTTT TGCTATGAGC AGGAGGGCGC AACTCTCATC CTGGGTGTAT 180
ATCCGGACAG CTCTGCTGGG TATCATTTAG GATATTCTTG GTTGTAAATA CAGCTGCTGC 240
TTGACTTAGG GTGGACCTAC ATCCCGATAA ACCCAACCTG AATAGAAAAT GCTGAAAGCC 300
GAAAATACAT TTAATGTCTG CAACACAGCA GACGGTGCCT GACTTAGGAT TGTTTGATTT 360
ACCGGCTTTC AGCTTTACCA TGGTGCCAAA GCGATAGGCT TTCAGTAGAA AACATAAATA 420
AATGGTAAGG AGCTTCCTGA CTTACGATGG GATTACCCAT CGTAGGTCGG AAAATTCGTG 480
TCAAGCATAA GTCAGTCGGG GACTGTCTGT AAGAGAAAAC CCAACCCAAA CTTGCTTAAG 540
CAAAACACAG GGTTTTGGGG GGCTCTTGGA ACTATGCAGC TTCTCGATAG CTTCAGGCAA 600
GACCTAATCC AGACTGAAGC ACATGATCAG GACTCAGCTG CCGAGTCTGC CGAGTCTGCC 660
GAGCTTTTTA TTGTTTTCTT GGCGGTGGTC CAGTCTGGAG GACTCTCCTT ATGGACCCAA 720
GACGGGTGCC AGGCGCTCCA GGGACTCCAG ATGGAAATAT GGAGATGGAA ATGGTTTCAC 780
GGTTCCCAAG GGAAGTCCTG AGATGTGCTC TGACTGGAGC CACTGAGGTC ATGTGCCCAC 840
ACTGAACCAA TCACTGTGGC CAGGGAGGCA GTGTGCTGAT TGGCTTAGGT CTGGACCATG 900
GCCTCCCCTC TGGAGGCTCA TTGGGTGGAG AGTAGGGGAG GGGTGGGCCC TTGACGGAGG 960
TTACTTGAAC CCGGCTGGGT GGTCAGTGAA GGTGGGAGTG AGTGGATCAG CCCCATTCAT 1020
TAGGGCCCTC ACTGGGATCA GAGCTTGGTT CCCCTCAGGG AGTGTCTGAG ACTCCTCCCT 1080
GTGTGATCCC TGCGGGGTGT GTGTGTGTGT GGCCATAGGG CGGTTGTGGC CTGAGCACTT 1140
TTGCCAGCAC CGCAGGTAGG TTCTTTTGTC CACACATGGG GATGTCCTGA CAGCTCCCGC 1200
CCCAGGGTCT GCCTGAACCC CACCCTGGGC CGCCTCCCCA TCGTTTCTCT CCCTGTGGCT 1260
ACCCTGTGAG ACCATCTCAT GTGGACCTTC CCCTCCTGTC CCCGGGAGGC CTGGGGATCT 1320
GGGCTGGGAC CCAGAGGTGC CCAGGTGAGG CGAATCAGGC AGTCCTTGTG GGCAGGTGGG 1380
GCTCCGGGGG AGTGGAAAGG GTATGCGGGC GCCAGCTGTG TCCCATCCTG GTGGTCTGAA 1440
AGAACAGGAA GGGGCCCAGG ACAAGGGGCC 1470
|
| |
|
|
|
