| Tag | Content |
|---|
EnhancerAtlas ID | HS101-02356 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:115677400-115679110 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr1:115678990-115679001 | ACAGATAAGAA | - | 6.14 | | Gata1 | MA0035.3 | chr1:115678990-115679001 | ACAGATAAGAA | - | 6.62 | | RREB1 | MA0073.1 | chr1:115677612-115677632 | GGGTAGGGGGTGGTGGGGAG | - | 6.4 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I115133 | chr1 | 115675635 | 115679109 |
|
Enhancer Sequence | CTTCAAGAAA CCCCCATGAC AAGAGGAAAG CTTGGTTAGT CTCAGTCTTA TGGAAACAGA 60
ATCTATGCTA GCCTAAGTCA TTTCTTAGAG ATCTGGAGAA TGAAAGTCAG TGGAACGTCC 120
CTAGGCACAC ACACATGTGA GTATCTCAGT GTAAACGTAT CTGCAGACTC CACCACAACC 180
CAGAAGTCCT GTGAGTGTGG GGCAAGCATG GCGGGTAGGG GGTGGTGGGG AGAGCGCCGA 240
GTGTGGGGAG ACCGAGGGAT CAGGGAGGAA AGCACTGCCT CCCCTTCCTG GAGAGTCCAG 300
TTGGAAGAAC TCATGGGTCA TGGCAGTAGA AAGTGCTACT TTTAGTTTCC TTCAGGATGT 360
AGATGCCATT TAAAGTCAAA CTATTTCCTA ATACTGGTGC CCAGAAAATG ATTCATTGGA 420
GAATGCTGAT GTTGTTTTCT GTGCCCGACA TGAAGCAGTG TGATGCTGTT TCAGAGCAGA 480
GGATATTGGC CTGAAGGGCT GTAACTCTGT GCTGTCCCCA AAGGCCGTTT CTGGGCAGTG 540
TTTATCTTTT GTCTGCCTGA GACTCTCTGT GTGGCTCACT CTTCATCGTG ATTCTTTGCA 600
TGCCTGTAAC ATGTGTCATC TACACGTATT CTTTTGGCAC CCATCACCTA CAGTTTTGGT 660
TACTTCCCTT AGAGGCTTGT GTTTGTGTCT GGGGGTGTGT TACTTTCTTT GCTTCCCCAG 720
ACCCTGGATC CATATTCAGG AGTCCCTGCT CTGACACTTT GTGCTATGTG AACTTCGACA 780
AGCCACGAAC GTCCCCACAC TTCTATTTCC TCACCTGTAA AATGGGAATG ATGACATCTG 840
ATGATAAGCA ACCATGGCCA ACTTATCTAA CAGAAATGAA GGTCCAATGC CAATATTGGA 900
GAATGCTTTG TAAATTCCGA ATTGTAGTGT TCAGTGAGAA ATTGATAACA TTTTCTTCTT 960
GTAAGGACTG TACTTCATAG ATTTTTAATG GCTGTCTCAC ATCGCAACCC CAAGATAACA 1020
CACTGCTGAG CAAATAGGAG GAGCTCAATA AATAATTGTA GAATGTGATC ATCGTTGTTC 1080
TCATCTTTAC AAATTCCTTA TTAATGCCGT TTTGTTGCTG CCAGATAACT CATTGTCTTC 1140
CCATGCTGAC ATTATATAAG TCTGGGACAC ACATGAACAT GGGAAGACAT CAGAAAGTTA 1200
CATAACTGAC CAGTAGAGAA TAAACATCAG TTACACATAA AGGTTAAGTG CATTTTAGAG 1260
GTTAGAAAAA GTGATGAGTG AATAATTGCG ATAGGAAAGT GGTTTGTGGG AACAGCTATA 1320
AGATATAGAT TGAGGTAGGT GGGATTGGGG AAGCTGCTTT TATCTAATTA AGAAGACCTT 1380
CAAGAGGAAG TGGATTTTCA GGAGCAGGTA GACGAGAGGG CAGAATGGGC TTGGTGAAGA 1440
GGTGGCCAGA GAACATTCCA GACACATGAG TATCCTCCGA AGGCTGTGGG GCAAGATACC 1500
TTCAGGGTGG TTTGCCCCTC TTGACAGTTG GAATGGCTAG AGGGGTGTGT GTGTATGTGT 1560
GTATAGACAT AGGGAAGCGG AGGGCAAGGG ACAGATAAGA AGGGTGGGAA AGAGGTAAGG 1620
GAGACCTGCT GGGGGTGATG AAGACAATGT AAGACTGATA ACCTTCAGGT GTGAGATGTT 1680
TTGGAGGAGC CCTGTTGAGA TTTCTTTACA 1710
|
