| Tag | Content |
|---|
EnhancerAtlas ID | HS133-23756 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr4:6933470-6934940 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr4:6934443-6934458 | GGGCTCAAAAGGTCA | + | 6.7 | | Nr5a2 | MA0505.1 | chr4:6934426-6934441 | TGTGGCCTTGAACTC | - | 6.65 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27664 | chr4:6927858-6933966 | Fetal_Intestine | | SE_28549 | chr4:6927396-6934981 | Fetal_Intestine_Large |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH04I006924 | chr4 | 6926250 | 6933811 | | GH04I006932 | chr4 | 6934108 | 6951477 |
|
Enhancer Sequence | GTTCTTAAAT ATGTTTCTCA TCATACATTC TTTAAAAAAA AATTGACTGA GCACCTGCCA 60
TATGCCAAGG CACTGTTCTA GGTGCTTGGG ATTCATTTGT GAACAAAACA GAGCCCCTGT 120
CCTCGCAGAG CTTAAGTTCT AGCAGAGGGT GCTGATGGTA AACACAGTGA GTAGATGGAG 180
GATATGTGTT GGCAGACTTA AGAGCTACGG AGAAAGCCAG CAAGCAGAGG TGGTACGAGG 240
TCCTGGGAGG AGCGGAGAAG ACAAGTTACA CAATGAATAG ACTGGTCAGG ATAGGCCTGA 300
AGGAGAAGAA GAGATTGAAG CAAAGACTTG AAGGTGGCCA GGCGGGTGGC TCACGCCTGT 360
AATCCCAGCA CTTCGGGAGA CCAAGGTGGG CAGATCACCT GAGGTTGGGA GTTCAAGACC 420
AGCCTGGCCA AGATGGTGAA ACCCTGTCTC TACTAAAAAT ACAAAAATTA GCTGGGTGTG 480
GTGGCATGCA CCTGTAATCC CAGCTACTCG AGAGGCTGAG GCAGGAGAAT TGCTTGAACC 540
ATTCGGGCTT GAACCCTGGC AGAGGTTGCA GCGAGCCAAG ATCGCCGCCA CTGCACGATC 600
TTGGGCGACA GAGCAAGACT CTGTCTGGAA ATTAAAAAAA AAAAAAAAGA CTTGAAGATG 660
TCAGTGACAA AGTTAACCAA GCAGGTACTT GGAAGGAGAG TGATCCAGCA AGGGAGAAGG 720
ATGCAGGCAG GCCTGATGCA TTTGAGCACA GATGCCCTGG GGATGGACAG AGAGAAGGAA 780
GGGATAGGGT CAGTGGGACC AGATTCTGTA TGGGCATGTA GGCCACTGTG TGATGTTGGC 840
TTTGACTTAG ACTCAGTGGG GAGCCACTGC AGAATTTTTG TCTTTTCGAG ATGGGGTCTT 900
GCTGCATTGG CCAGCCAGGA GTCCAGTGGC CATTCACAGG TGCAGCCATA GCGCAGTGTG 960
GCCTTGAACT CCTGGGCTCA AAAGGTCATC CTGCCTCAGC CTCAGAATAG CTGGGCCTAC 1020
CACACCACTG TGCCTGGCTC TACTGCAGAA TTTTGAGCAG AGGAGTTGCC GTGGTGTTTT 1080
GCTGCTGCAT AACAAATAAC CACACATTTG GTGGCTTGAA ACAACATGGC TGTCCATCAT 1140
GGTGTGGCTG GGTTCCCCTC GGGCACTTAT CAGGATGAAA CAGCATGTTG GCGGCTGTGT 1200
CCCCGTCCCA GTCTTGGCTA AGGAATTGTC TGCTTCCAGG CTCACTGAGG CTGTTGGCAG 1260
AGCTCGTTGT GGCTATAAAC TGAGCTCATC ATTTCCCTGA TTGCTGTCAG CTGAGGGTCA 1320
CTTGCAGCTC CTAGAAGTCA TCCAAATTCT TTGCTGTGTG GCCCCTCCAT ATTGAAAACC 1380
AGCAACAAGG CTTCTTTTGT GTGGAGTCCA TCTCACACTC CAAATCTCTT CCCAGAGAGA 1440
ACACTGATTG CTTTTAAGGG CTCACTGAAA 1470
|
