| Tag | Content |
|---|
EnhancerAtlas ID | HS042-04022 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:228995330-228997180 |
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 | chr1:228995926-228995938 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:228995930-228995942 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:228995934-228995946 | GTTTGTTTGTTT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr1:228996186-228996201 | TGAACTCCTGACCTC | - | 6.22 | | RREB1 | MA0073.1 | chr1:228995967-228995987 | GGGGGTGGGGTGGGGTGTGG | - | 7.06 | | RREB1 | MA0073.1 | chr1:228995962-228995982 | TTTTGGGGGGTGGGGTGGGG | - | 7.13 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23450 | chr1:228995808-228996099 | Colon_Crypt_1 | | SE_23450 | chr1:228996189-228997694 | Colon_Crypt_1 | | SE_27943 | chr1:228995103-228998116 | Fetal_Intestine | | SE_28861 | chr1:228994670-228998359 | Fetal_Intestine_Large | | SE_52925 | chr1:228994663-228998395 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I228859 | chr1 | 228994940 | 228998147 |
|
Enhancer Sequence | GAGAATTGGT ATGGGTGTGG TCACCGAAAT CAGCTAAGGA GGCCCCTAAT CTGTGCTGTC 60
GGCTCTCCTG ACTACCTAAG TGCAGGAGTT GGGTCTGTAA ACCACAGTGA CTGAGACAGA 120
TCTCAATTGA TTTCGAGGCT TATTTTGCCA AGGTTGAGGA GGCACCAGAG AAAAAGAAAC 180
ATAAATCACA GTAGAATCTG TATCCTATGC TTTTTCCAGA TAGAGTTTTG GGAACCTCAG 240
TGTTTAAAGG GGAAAGAGCA ATCAGGAGGG GAAGAAAAAG GAAAAATAAA AGGAGGGAGG 300
GTAGGCAATG AGACAAGTGG TTACAATTCT TGTGAGGCTC TGTGAATCTA CATTTTACAC 360
CTGAAAAGAA AGCGGAGGAG TCAATTAAGC ATTAGTCTGG CACTCAGCAA ATCTACATTT 420
TACATAAGAG AAAGTCAGCC TGCGAAATTA CAGCTGTCTT GGAACAAAAG GAAGGGAGTT 480
TTTGCATGAC TCAGTTTCCA AGCTTAACTT TTCCCTTTGG CATAGTGAGT TTGGAGTCCC 540
GAGATTTTAT TTTCCTTTCA CAGGCCTTTC CACTGTGGTG TTTTCTTCTG TTTTTTGTTT 600
GTTTGTTTGT TTGTTTTTTG CTTTTTGGGT TTTTTTGGGG GGTGGGGTGG GGTGTGGGAC 660
AGAGTCTCAT TATGTCCCCT GGGCTAGAGT GCAATGGTAC GATGTCAGCT CACTGCAACC 720
TCTGCCTCCC AGGTTCAAGC GATTCTCCTG CCTCAGCCTC CTGAGTAGCT GAGATTATAG 780
GCACATGCCA CTACACCTGG CTGATTTTTG TATTTTTAGT AGAGATGAGG TTTCACCATG 840
TTGGCCAATC TGGTCTTGAA CTCCTGACCT CGTGATCCAC CCACCTCAGC CTCCCAAAGT 900
GCTGGGATTA CAGGTGTGAG CCACCACGCC CGACCTTTTC TTCTGTTTAT GCAGTGGCAT 960
GGAGCAGTCC CTCTAAGAGG GCTGACCCAG GTATGAGTCA TTCAGTCAGC CTGAGGGTCC 1020
AAGGGCTGCT CCATGGTGAG GCAGACATCC AGAAGGGTCC AGAGGGAGAA TCTATGGCAA 1080
GAGACAGCAG TCTAGAGGGA TGGAAGTGGT GGCAGAAAAG CTGGCTTTTA AAAGGCAAGT 1140
TTTTATTCTA GGCTGACTTT CTCTTATGTA AAATGTAGAT TTGCTGAGTG CCAGTGAATT 1200
TATAATTTTA GAAACCCATC AGGGAGTTTC TAGATGAGTT TCTAAGAAGT CTAAGAAATG 1260
TCCAGGAAGG CCCTTAGCCA CCTCGTGGAA ATTGGGAGAG AAGAAATGTG TGCAGAGAAA 1320
AGAGGGATTT TTGATGCAGA GAAAAAGAAC AGGTGTGTCC CGGCTGCTGG CTCTGAGTAA 1380
CCCGTCTAAT CTCACTGTAC AGAACGTACC TGCACTTTAT ACTAACAATG AGTGCCATTC 1440
AGCGTGCCAT TTATGATGTT CACAGTGGCC TTCCTTGGTG TGGTCCCTGA AGCCCTGCAA 1500
AGCAGGGACT GTGCGGTCTG AACCAAACAG GGGCCCCTGG GAATAGGGTA GCGTGTTCTG 1560
ATACCTGAGC TGGTAGTAGA GTCAGAGCAA GAACAAAAGC CCCAGCGAGC AATCTGGGTT 1620
CAACCCCTGT CACCTTAGCT CACGTGCCTG CATTGTGAAG TTCACGGTAA TAGCTTGACT 1680
GCATTCTCGC CATGGTTCTG GGTCAATAAA TCAGTCAGTA AGCACTGGGT GAGTAAGTAG 1740
TGCAGAGCAA AGTCTGAGCT TGGTGCCACA AGTGGATAAA AAAGAAATAG ATGACTCAAC 1800
CTCTGCTTAT AGGGAGGCTC TGATCTAGCT GAGATAGCAC AGAAATATTT 1850
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