| Tag | Content |
|---|
EnhancerAtlas ID | HS076-34377 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr2:212631080-212632100 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr2:212631883-212631894 | TTTTATTGCTT | - | 6.32 | | NFYA | MA0060.3 | chr2:212631589-212631600 | TCTGATTGGTC | - | 6.14 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I211766 | chr2 | 212631021 | 212631989 |
|
Enhancer Sequence | TGTAACCAGT GGTCTCTCCC CTTCCTCCTC TCTAAACTTT GAAATAAAAG TCCTGAATGA 60
GGGAACACCA ATAGGAGAGG AAAGACACAT GTGAAACATC TTGGTAAATG TTATGAAAAG 120
GGAAAGCTGA ATGTCTGCAC ATGTTTTCAG TTATTCATAA ACATCTTCCT TTTGCTTTCT 180
AGTTTTCAAG TGATGAGAAA TTAGAGAAAA AAAGGGAAAA TAGTTCCTTA AGTTCTATTT 240
AATTGTGAAA CTGAATTCTA TGAAACACTT TCATTAGTAA ACAAGGATGA ACTTGTGAGT 300
TGTGATGAAA TCTGTGAATG ATGGTTGTGA GGCAGGAGAA CAGGGTCTGA AGGCAGGGAA 360
CCTAACGCCG ATCTGTGCTG ATTTCCTAGA ATGGAATCAA AAGGAAAACC CCACCTCTCC 420
ACTCTCGAGT AACAAAAGGA TCAAAGGCTA CTCCTTTTGC AACACCCCAC TCCCCCATTT 480
CTGCATTGTG GAGGAGAAAG TAAAGTACTT CTGATTGGTC TGCTCCTGAA ACCGGTCAGA 540
CTGGTCATGT CGGCCTTGTC TTCATTTGCA TAGGGGTGTG ACTTGGTAAC TTCACTTCAG 600
TCTGTTTGGT CACCTTCCAA CACCAGTCTG ACTGGTTGGG GGCCACCACT TCATTAATAG 660
GGTGTAAAGC AAGTAACCAA TGGGAAACCT CTCCAGGGTA TTTAAACATC AGAAAATTCT 720
GTAACCAGCA CTCTGGAGTC GCTTGCTCAA GGCTACTCCC ACTCTGTGTA GAGTACTTTT 780
GTTTTAATAA ATCTGTGCTT TTATTTTATT GCTTTGTTCG TGCATTTTTC CCAATTCTTT 840
GTTCAAAACA CCAAGAACCT GGTCACCCTC CACTGGTAAC AGAACACTTA CATAATTACT 900
CTCACCCATT ACAGAGTAAA CAAAAATAGA AGAGAGTAAT ACTGAATAGA GTCAGTGTAA 960
TTGTCATTCA ATTTTACACA GTTACTTTAA ACACCAAATA TACAATCAGG GTTTTATGTT 1020
|
