| Tag | Content |
|---|
EnhancerAtlas ID | HS088-23091 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr17:38341130-38342540 |
Target genes | | Number: 24 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr17:38341715-38341730 | AAGGTCAGGAGTTCA | + | 6.04 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23388 | chr17:38341243-38341658 | Colon_Crypt_1 | | SE_25171 | chr17:38341241-38341719 | Colon_Crypt_3 | | SE_26964 | chr17:38340314-38341733 | Esophagus |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I040185 | chr17 | 38341641 | 38341790 |
|
Enhancer Sequence | AAGTGATTCT CATGCCTCAG CCTCCTGAGT AGCTGGGATT ACAGGGGTGC ACCATGCCCA 60
GCTAATTTTT GTACTTTTAG TAGAGATGGG TTTCACCATG TTGGCCAGGC TGTTCTTGAA 120
CTCCTGGCCT CAAGTGATCT GCCTGCCTCA GCCTCCCAAA GTGCTGGGAT TACAGGTGTG 180
AGCCACTGTG TCTGGCTTCC AATATGGTTT TATTTCAGCT CCTTTCTCTC ACTGAAGGGT 240
GGCACAAAGC ACTGTCTCCA GTCACTTTTT TGTCCATTCT CCCATTCATT TGTCTGATAA 300
TCCAGTGGTG TACTGGTAAA TATTTAACAA CCAGTGCTGC AGGAGAAAGA GCCCTGATTT 360
GTAGCTTTTG CTGATTCCTA CAGTGTAAAC TCTGTCACCA TGGCTGATTT CAAGCTACCA 420
ATGTGACAAC ACTGAAAGAG GAGTTGGGAA GAGACATGCA GCACAGGCTG TTATGTAGTA 480
TCTCCACCAT ACAGTAGATG TAGTAAAAGG TAGTAAAATG GCTGGGCAAG GTGGCTTATG 540
CCTGTAATCC CAGCACTTTG GGAGGTCAAG ATGGGTGGAG CACTTAAGGT CAGGAGTTCA 600
AGACCAGCCT GGCTAACATT GTGAAACCCT GTCTCCACTA CAAAAAAAAA AAAAAAAAAA 660
AAGGCTGTGT GCCAAGGCAG GCAGATCATG AGGTCAGGAG TTTGAGAGCA GCCCGGCCAA 720
TATGGTGAAA CCCTGTCTCT ACTAAAAATA CAAAAATTAG CTGGGCGTGG TAGGGCGCTC 780
CTGTAGTCCC AGCTACTTGG GAGGGTGAGG CAGAAGAATT GCTTGAATCC AGGAGGTGGA 840
GGTTGCAGTG AGCTGAGATC ATGCCACTGC ACTCCAGCCT GGGCGACAGA GTGAGATTCT 900
GTCTCAAAAA AAAAAAAAAA AAAAAGAAAA GAAAAATTAG CTGGGGGTGG TGGTACGTGC 960
CTGTAGTCCC AGCTACTCAG GAGGCTGAGG CAGGAGAATT GCTTGAACCC AGGAGATGGA 1020
GGTTGCAGTG AGCTGAAATC ACCTTACTGC ACTACAGCCT GGGTGACAGA GCGAGACTCC 1080
GTCTCTAAAG AAAAAAAAAA AGGCCGGGTG CGGTGGCTCA CGCCTGTAAT CCCAGCACTT 1140
TGGGAGGCTG AGGCAGGCAG ATCATGAGAG GCAGATCATG AGATCAGGAG TTCGAGACCA 1200
GCCTGACCAA CATGGTGAAA CCCCATCTCT ACTAAAAATA CAAAAATTAG CCAGGCATGG 1260
TGGCACATGC CTGTAATCCC AGCTACTCAA GAGGCTGAGG CAGGAGAATG TCTTGAATCC 1320
AGGAGGCAGA GGTTGTAGTG AGCCAAGATT GCATCACTGC ATTCCAGCCT GGGTGACAGA 1380
GTGGACTCCG TCTCAAAAAA AAAAAAAAGG 1410
|
