| Tag | Content |
|---|
EnhancerAtlas ID | HS179-03493 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:228973350-228974750 |
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 | AAAACCCATG TCAGGTTGCT CCCCTGAGCA AGGCCAAGCT CAGTTTTCAC CTGGTGGTCC 60
CATGGGGAGC TTCCTGTGGC TTAGTGTTTG CGTCTGCCAT TTGCTATCCC TCCCCAGCAC 120
ACCTTCCTGT GGATGGAACT TGCCAGAACT TCCTCAGCAA CCCTGAAGAG GAAAGCTGGA 180
GGCCCCAACA GACGCAGAAG TGGGCTGCAC TGCTGTGCTT CCATGGGGCA GTCAGGGCTC 240
AGGGCCCCAG CAGCAGGCCA AACCCCAGCC CAGCTCCCTT GCAAACCTCC TCTGTCATGT 300
ACCCTGGGAG TCAGGTCCAA CCCCACTATG TCACAACTGA GGAAACAGAG GCCCCGAGAA 360
GTTCAGGGAG AGCTGGGGTC AAGATGCTAG ATCCTGCCTC TGGGTGTGGT GGCTTTTGTT 420
CTTGTCATCC GGTGGGCACT GGGCCTGCCC CGCACAGCTC CTTCACCCCG GAGAGGTGAC 480
AGCAGACTAC ATTAGGCCCT GCCAGGCCCA AAGACTCCAG CCTGTTAATC TTTAACCAGA 540
GCTCTGGACA AAGGTAGCCC TTCTGACCTC CTGAGAGTTT CTGAATAGCT CGGAGGCTTC 600
TGTGACAGAG CCACACGTTA GCAATGACAT ATATTTAGTG CAGGGAGGCA TGTTGAGTAC 660
AGTTCTAAAT TCTGTTGTGA ATTGTGCCCA GGGAACAAGC ACAGAGAACA TTTTCACCAT 720
GGATATGTAT GTACTTGTAA GAAGCAGCTG GGTGGTTCCT TCAGCAATCT GCTGAGCTGT 780
GGCGATTACA TCACACACTG GTGCAAAGGC CTTGAACCAT TAATGTGCTG CCTCTGCGAG 840
GGTGACCAGG ATTCCAGCAA TGAACAGAGA AGGTGCTTGT CCCCACTGCT CACTGGGTGC 900
CTTCAGATTC TTAACTTTTG TCTTTTTCTT TTTTCTTTCA CTTCTTACCT GTATCTATAA 960
AACAGGACTC TGTTTGCTTT GAAAAGAGCC AGAATGACCT CAGGGGTCAG TGACTCATGC 1020
TGTTGGCTCT GTGAACACAA TCGAGTGCCC CTTACGTAAG AAGCTCCTGC TATCTGAGGG 1080
AAGGGAGGTC CGAGCCATTA TTCCTTGGTT ATAAACACTC CATGTGGTTT TGTTTGGTGG 1140
TTTTAAAAAA GGTGTGTCCA CAGGGTTGGT GTTCTAGAAT CGTGGGCAGA AAGAAGTCTA 1200
GCTCCTTTCA TCCAAGGTTC TAAAGGGTTC TCTGAGCTGT AACTCAGCTC TAACTGGACA 1260
AAGAGGCAAC AATTCCCCTC ATTTCCTGTG CGCTGTCACC ACAGGAGGCT ACACTTAAGG 1320
AGGTCAACTC AAGTTGTTTG GACCAAGCTT CCGCAGTTGT TCCCATTATC CTGTTTGAAT 1380
CCATTCACTC TTACACTGGC 1400
|
