| Tag | Content |
|---|
EnhancerAtlas ID | HS044-01225 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:228973400-228974760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:228974358-228974369 | AGTGACTCATG | + | 6.14 | | HNF1A | MA0046.2 | chr1:228973872-228973887 | TGTTAATCTTTAACC | - | 6.36 | | HNF1B | MA0153.2 | chr1:228973873-228973886 | GTTAATCTTTAAC | - | 6.18 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23450 | chr1:228971657-228975640 | Colon_Crypt_1 | | SE_27943 | chr1:228970281-228975761 | Fetal_Intestine | | SE_28861 | chr1:228970139-228975730 | Fetal_Intestine_Large | | SE_52925 | chr1:228971171-228975530 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I228834 | chr1 | 228970561 | 228975769 |
|
Enhancer Sequence | CTGGTGGTCC CATGGGGAGC TTCCTGTGGC TTAGTGTTTG CGTCTGCCAT TTGCTATCCC 60
TCCCCAGCAC ACCTTCCTGT GGATGGAACT TGCCAGAACT TCCTCAGCAA CCCTGAAGAG 120
GAAAGCTGGA GGCCCCAACA GACGCAGAAG TGGGCTGCAC TGCTGTGCTT CCATGGGGCA 180
GTCAGGGCTC AGGGCCCCAG CAGCAGGCCA AACCCCAGCC CAGCTCCCTT GCAAACCTCC 240
TCTGTCATGT ACCCTGGGAG TCAGGTCCAA CCCCACTATG TCACAACTGA GGAAACAGAG 300
GCCCCGAGAA GTTCAGGGAG AGCTGGGGTC AAGATGCTAG ATCCTGCCTC TGGGTGTGGT 360
GGCTTTTGTT CTTGTCATCC GGTGGGCACT GGGCCTGCCC CGCACAGCTC CTTCACCCCG 420
GAGAGGTGAC AGCAGACTAC ATTAGGCCCT GCCAGGCCCA AAGACTCCAG CCTGTTAATC 480
TTTAACCAGA GCTCTGGACA AAGGTAGCCC TTCTGACCTC CTGAGAGTTT CTGAATAGCT 540
CGGAGGCTTC TGTGACAGAG CCACACGTTA GCAATGACAT ATATTTAGTG CAGGGAGGCA 600
TGTTGAGTAC AGTTCTAAAT TCTGTTGTGA ATTGTGCCCA GGGAACAAGC ACAGAGAACA 660
TTTTCACCAT GGATATGTAT GTACTTGTAA GAAGCAGCTG GGTGGTTCCT TCAGCAATCT 720
GCTGAGCTGT GGCGATTACA TCACACACTG GTGCAAAGGC CTTGAACCAT TAATGTGCTG 780
CCTCTGCGAG GGTGACCAGG ATTCCAGCAA TGAACAGAGA AGGTGCTTGT CCCCACTGCT 840
CACTGGGTGC CTTCAGATTC TTAACTTTTG TCTTTTTCTT TTTTCTTTCA CTTCTTACCT 900
GTATCTATAA AACAGGACTC TGTTTGCTTT GAAAAGAGCC AGAATGACCT CAGGGGTCAG 960
TGACTCATGC TGTTGGCTCT GTGAACACAA TCGAGTGCCC CTTACGTAAG AAGCTCCTGC 1020
TATCTGAGGG AAGGGAGGTC CGAGCCATTA TTCCTTGGTT ATAAACACTC CATGTGGTTT 1080
TGTTTGGTGG TTTTAAAAAA GGTGTGTCCA CAGGGTTGGT GTTCTAGAAT CGTGGGCAGA 1140
AAGAAGTCTA GCTCCTTTCA TCCAAGGTTC TAAAGGGTTC TCTGAGCTGT AACTCAGCTC 1200
TAACTGGACA AAGAGGCAAC AATTCCCCTC ATTTCCTGTG CGCTGTCACC ACAGGAGGCT 1260
ACACTTAAGG AGGTCAACTC AAGTTGTTTG GACCAAGCTT CCGCAGTTGT TCCCATTATC 1320
CTGTTTGAAT CCATTCACTC TTACACTGGC CATGCAAATA 1360
|
