| Tag | Content |
|---|
EnhancerAtlas ID | HS134-14546 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr12:89766240-89767280 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr12:89766479-89766491 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:89766483-89766495 | AAACAAACAAAC | - | 6.32 | | HNF4G | MA0484.1 | chr12:89766805-89766820 | TGGCCTTTGTTCTTT | - | 6.14 | | MAX | MA0058.3 | chr12:89767024-89767034 | ACCACGTGCT | + | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_27644 | chr12:89763300-89771362 | Fetal_Intestine | | SE_28566 | chr12:89761572-89775819 | Fetal_Intestine_Large | | SE_35929 | chr12:89761762-89771214 | HMEC | | SE_38298 | chr12:89761862-89771214 | HUVEC | | SE_41177 | chr12:89766532-89767330 | Left_Ventricle | | SE_48925 | chr12:89766309-89767299 | Right_Atrium | | SE_50215 | chr12:89766250-89767304 | Sigmoid_Colon |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I089368 | chr12 | 89761900 | 89775589 |
|
Enhancer Sequence | GGGCAAGAAG GTTGAAGACT AGGCAGGGAG AGAGACCTGA ACTAAAGCAG GAGAAGGCAA 60
GGTGTAGTAT ACACATCATG GAGACATGTA TAAAGCATTC CTGGAACCCA GAGGAACCAG 120
GAAGTGCTGC TCATAAAAGA TGCTTTTTGA ACTAGATCTT GAAGAGTGAG TAGCCCGAGG 180
AGTTTGGGCT TGCGAATTCT AGATAACAAG AACAGCTTGC CAAAAGGGAT AAAGTTGTGA 240
AACAAACAAA CAAACAAAAA ACAGGGTTTG GAGCCAGGAG GACTTTGGTG TGAGTGGTGT 300
TTGGCCATTC TGCCTGGTGC CTTCCTTTGA ATTTAGGTTC GACCCCCTGT GGGGGCCACA 360
GAGAGTCACC TGCAGCTCAG TCTTACCCCA GGTGCTGGGC CCAAGTCTGC TCTTAGAGGA 420
AATGTAAGTA GCTTATATCA CTCAGTATCG GGTCAGCTAG GCTCTGGGTT CTGTTCTGAG 480
CTCCTGCTCT ATTTCTAGCT GTGAAGTTTC CACTTGATTC CTGTCACAGG CTCTACCTTG 540
TATTCCAGTT CAAATAACTG GGCTTTGGCC TTTGTTCTTT CTTCTACATT CTGCCTCTAA 600
GTTTCTCTAA GACTGGAATT TTGCCTTTCC TTATCAGTCC TTCCTAGAAC TTCAGTCCCT 660
CCCAGAACTT CAGTCCCCTC CTTGGCCCTG GGGCCTCACT CCAGGCTGCT TGATCCACTT 720
ATGGTTATTG CTTGCTGGGT TCACCTTCTT CTCCTTTCTG CAGGTGGAAC ACAGACTGAT 780
GACAACCACG TGCTGAGATC CCCTGTTACT GCCTAGACAC AAATTGCTAT CTAGGTCCTG 840
TTTCACTGCC TGGCAGAACT GCCTTGCTAC TTCTGGTTTG GCTCGCCATT GCCTGAATTC 900
CTAAACTCCA TTCTGAATAT TACTAGTGAA AAATGCACGG CAGGGCGCAG TGGCTCATGC 960
CTGTAACCCC AGCCCTTTGG GAGGCTGAGG CAGGTGACTC ACCTGAGGTC AGGAGTTCGA 1020
GACCAGCCTG GCGAACATGG 1040
|
